A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998533



Internal ID19158069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75600071hg38UCSC Ensembl
Innerchr3:75421158..75649222hg19UCSC Ensembl
Innerchr3:75503848..75731912hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38228065
hg19228065
hg18228065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3601985, nssv3601987, nssv3601982, nssv3733021, nssv3733022, nssv3601983, nssv3601986, nssv3733023, nssv3601984
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)nsv998533
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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