A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750284



Internal ID15697554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73874102..73874904hg38UCSC Ensembl
Innerchr10:75633860..75634662hg19UCSC Ensembl
Innerchr10:75303866..75304668hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38803
hg19803
hg18803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551525
Supporting Variants
Samples
Known GenesCAMK2G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750284
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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