A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006264



Internal ID19095482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77738348..77893768hg38UCSC Ensembl
Innerchr3:77787499..77942919hg19UCSC Ensembl
Innerchr3:77870189..78025609hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38155421
hg19155421
hg18155421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596210
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)nsv1006264
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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