A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747658



Internal ID15694928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49115184..49115894hg38UCSC Ensembl
Innerchr10:50323229..50323939hg19UCSC Ensembl
Innerchr10:49993235..49993945hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38711
hg19711
hg18711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550818
Supporting Variants
Samples
Known GenesVSTM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747658
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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