A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581774



Internal ID16369183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:48187596..48266043hg38UCSC Ensembl
Innerchr2:48414735..48493182hg19UCSC Ensembl
Innerchr2:48268239..48346686hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3878448
hg1978448
hg1878448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150445
SamplesNINDS_46
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581774
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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