A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557958



Internal ID16345367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29786695..29945837hg38UCSC Ensembl
Innerchr12:29939628..30098770hg19UCSC Ensembl
Innerchr12:29830895..29990037hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38159143
hg19159143
hg18159143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175824
SamplesNINDS_133
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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