A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752192



Internal ID16046148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86181240..86249143hg38UCSC Ensembl
Innerchr10:87940997..88008900hg19UCSC Ensembl
Innerchr10:87930977..87998880hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3867904
hg1967904
hg1867904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551763
Supporting Variants
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752192
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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