A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707688



Internal ID19005969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9937318..9965411hg38UCSC Ensembl
Innerchr10:9979281..10007374hg19UCSC Ensembl
Innerchr10:10019287..10047380hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3828094
hg1928094
hg1828094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055089
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707688
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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