A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv717637



Internal ID16011593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:78184178..78201306hg38UCSC Ensembl
Innerchr1:78649862..78666990hg19UCSC Ensembl
Innerchr1:78422450..78439578hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3817129
hg1917129
hg1817129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546600
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv717637
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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