A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748921



Internal ID15696191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60042584..60054294hg38UCSC Ensembl
Innerchr10:61802342..61814052hg19UCSC Ensembl
Innerchr10:61472348..61484058hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3811711
hg1911711
hg1811711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551176
Supporting Variants
Samples
Known GenesANK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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