A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006121



Internal ID19095339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75590743hg38UCSC Ensembl
Innerchr3:75421158..75639894hg19UCSC Ensembl
Innerchr3:75503848..75722584hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38218737
hg19218737
hg18218737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3595032, nssv3595026, nssv3595004, nssv3733007, nssv3595033, nssv3595035, nssv3733008, nssv3601980, nssv3595022, nssv3733015, nssv3595020, nssv3595009, nssv3733018, nssv3594994, nssv3595041, nssv3733009, nssv3733016, nssv3594999, nssv3595001, nssv3595011, nssv3595025, nssv3595006, nssv3595012, nssv3733013, nssv3595017, nssv3595002, nssv3733019, nssv3595040, nssv3595023, nssv3595003, nssv3595000, nssv3595014, nssv3595007, nssv3595039, nssv3595031, nssv3595013, nssv3595042, nssv3595034, nssv3733006, nssv3733012, nssv3595028, nssv3594998, nssv3595038, nssv3595008, nssv3595029, nssv3595018, nssv3594996, nssv3733020, nssv3595019, nssv3595005, nssv3595024, nssv3601979, nssv3595016, nssv3733010, nssv3595037, nssv3595021, nssv3733017, nssv3601978, nssv3595010, nssv3595027, nssv3595036, nssv3733005, nssv3733011, nssv3733014, nssv3594997, nssv3595030, nssv3595015, nssv3594995
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006121
Frequency
Sample Size11257
Observed Gain0
Observed Loss68
Observed Complex0
Frequencyn/a


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