A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701951



Internal ID15091917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73802158..73847410hg38UCSC Ensembl
Innerchr10:75561916..75607168hg19UCSC Ensembl
Innerchr10:75231922..75277174hg18UCSC Ensembl
Innerchr10:75231922..75277174hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3845253
hg1945253
hg1845253
hg1745253
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517549
Supporting Variants
Samples
Known GenesCAMK2G, NDST2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701951
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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