A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696582



Internal ID15086548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1165203..1181073hg38UCSC Ensembl
Innerchr4:1158991..1174861hg19UCSC Ensembl
Innerchr4:1148991..1164861hg18UCSC Ensembl
Innerchr4:1148821..1164691hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3815871
hg1915871
hg1815871
hg1715871
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519106
Supporting Variants
Samples
Known GenesSPON2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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