A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740216



Internal ID15687486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1300624..1301363hg38UCSC Ensembl
Innerchr10:1342819..1343558hg19UCSC Ensembl
Innerchr10:1332819..1333558hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38740
hg19740
hg18740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549787
Supporting Variants
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv740216
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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