A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987708



Internal ID15934978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1539497..1609145hg38UCSC Ensembl
Innerchr4:1541224..1610872hg19UCSC Ensembl
Innerchr4:1512029..1580831hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3869649
hg1969649
hg1868803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593318
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)nssv987708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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