A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756066



Internal ID15703336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100192910..100198731hg38UCSC Ensembl
Innerchr10:101952667..101958488hg19UCSC Ensembl
Innerchr10:101942657..101948478hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg385822
hg195822
hg185822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552046
Supporting Variants
Samples
Known GenesCHUK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756066
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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