A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469714



Internal ID19063525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94686257hg38UCSC Ensembl
Innerchr1:95130666..95151813hg19UCSC Ensembl
Innerchr1:94903254..94924401hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3821148
hg1921148
hg1821148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001354
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)nssv3469714
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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