A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695086



Internal ID15085052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3484059..3502835hg38UCSC Ensembl
Innerchr4:3485786..3504562hg19UCSC Ensembl
Innerchr4:3455584..3474360hg18UCSC Ensembl
Innerchr4:3522755..3541531hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3818777
hg1918777
hg1818777
hg1718777
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516505
Supporting Variants
Samples
Known GenesDOK7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695086
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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