A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv914700



Internal ID15861970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102061304..102074850hg38UCSC Ensembl
Innerchr2:102677765..102691310hg19UCSC Ensembl
Innerchr2:102044197..102057742hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3813547
hg1913546
hg1813546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582554
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv914700
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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