A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465379



Internal ID19061198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72796875..72853816hg38UCSC Ensembl
Innerchr1:73262558..73319499hg19UCSC Ensembl
Innerchr1:73035146..73092087hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3856942
hg1956942
hg1856942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001105
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)nssv3465379
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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