A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001691



Internal ID19090908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75466940hg38UCSC Ensembl
Innerchr3:75427095..75516091hg19UCSC Ensembl
Innerchr3:75509785..75598781hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3888997
hg1988997
hg1888997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4775n100
Supporting Variantsnssv3733041, nssv3733039, nssv3733035, nssv3602026, nssv3733033, nssv3733042, nssv3733045, nssv3733047, nssv3733038, nssv3733044, nssv3602021, nssv3602024, nssv3602018, nssv3602028, nssv3733046, nssv3602023, nssv3602030, nssv3733036, nssv3733034, nssv3602014, nssv3602020, nssv3733040, nssv3602025, nssv3602015, nssv3602017, nssv3602022, nssv3602012, nssv3733037, nssv3602013, nssv3602027, nssv3733043, nssv3602016, nssv3602029, nssv3602019
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)nsv1001691
Frequency
Sample Size11257
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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