A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756067



Internal ID15703337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100194590..100198475hg38UCSC Ensembl
Innerchr10:101954347..101958232hg19UCSC Ensembl
Innerchr10:101944337..101948222hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg383886
hg193886
hg183886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552047
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)nssv756067
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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