A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744321



Internal ID16038277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20475220..20553102hg38UCSC Ensembl
Innerchr10:20764149..20842031hg19UCSC Ensembl
Innerchr10:20804155..20882037hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3877883
hg1977883
hg1877883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550148
Supporting Variants
Samples
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744321
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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