A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750275



Internal ID15697545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73799109..73898823hg38UCSC Ensembl
Innerchr10:75558867..75658581hg19UCSC Ensembl
Innerchr10:75228873..75328587hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3899715
hg1999715
hg1899715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551517
Supporting Variants
Samples
Known GenesCAMK2G, NDST2, ZSWIM8, ZSWIM8-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750275
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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