A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000399



Internal ID19089616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94687052hg38UCSC Ensembl
Innerchr1:95130666..95152608hg19UCSC Ensembl
Innerchr1:94903254..94925196hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3821943
hg1921943
hg1821943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3480435
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)nsv1000399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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