A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521143



Internal ID15101750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35624277..35647825hg38UCSC Ensembl
Innerchr10:35913205..35936753hg19UCSC Ensembl
Innerchr10:35953211..35976759hg18UCSC Ensembl
Innerchr10:35953211..35976759hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3823549
hg1923549
hg1823549
hg1723549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697812
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521143
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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