A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904162



Internal ID16198118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18003906..18062268hg38UCSC Ensembl
Innerchr2:18185172..18243534hg19UCSC Ensembl
Innerchr2:18048653..18107015hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3858363
hg1958363
hg1858363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581108
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)nssv904162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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