A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746849



Internal ID15694119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35638239..35644550hg38UCSC Ensembl
Innerchr10:35927167..35933478hg19UCSC Ensembl
Innerchr10:35967173..35973484hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg386312
hg196312
hg186312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550413
Supporting Variants
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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