A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701731



Internal ID15091697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98388419..98420094hg38UCSC Ensembl
Innerchr10:100148176..100179851hg19UCSC Ensembl
Innerchr10:100138166..100169841hg18UCSC Ensembl
Innerchr10:100138166..100169841hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3831676
hg1931676
hg1831676
hg1731676
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515723
Supporting Variants
Samples
Known GenesHPS1, MIR1287, PYROXD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701731
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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