A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466477



Internal ID19061773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94687706hg38UCSC Ensembl
Innerchr1:95130666..95153262hg19UCSC Ensembl
Innerchr1:94903254..94925850hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3822597
hg1922597
hg1822597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003354
Supporting Variants
Samples
Known GenesLINC01057
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3466477
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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