A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753976



Internal ID15701246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92689583..92690577hg38UCSC Ensembl
Innerchr10:94449340..94450334hg19UCSC Ensembl
Innerchr10:94439320..94440314hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38995
hg19995
hg18995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551933
Supporting Variants
Samples
Known GenesHHEX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753976
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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