A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652335



Internal ID15042301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73799109..73898591hg38UCSC Ensembl
Innerchr10:75558867..75658349hg19UCSC Ensembl
Innerchr10:75228873..75328355hg18UCSC Ensembl
Innerchr10:75228873..75328355hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3899483
hg1999483
hg1899483
hg1799483
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)nssv652335
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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