A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753969



Internal ID15701239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92689529..92690255hg38UCSC Ensembl
Innerchr10:94449286..94450012hg19UCSC Ensembl
Innerchr10:94439266..94439992hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38727
hg19727
hg18727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551929
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)nssv753969
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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