A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756037



Internal ID16049993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98523394..99122064hg38UCSC Ensembl
Innerchr10:100283151..100881821hg19UCSC Ensembl
Innerchr10:100273141..100871811hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38598671
hg19598671
hg18598671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552029
Supporting Variants
Samples
Known GenesHPSE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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