A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698468



Internal ID15088434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73799109..73873002hg38UCSC Ensembl
Innerchr10:75558867..75632760hg19UCSC Ensembl
Innerchr10:75228873..75302766hg18UCSC Ensembl
Innerchr10:75228873..75302766hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3873894
hg1973894
hg1873894
hg1773894
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517549
Supporting Variants
Samples
Known GenesCAMK2G, NDST2, ZSWIM8, ZSWIM8-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698468
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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