A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549096



Internal ID16336505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208472745..208508474hg38UCSC Ensembl
Innerchr1:208646090..208681819hg19UCSC Ensembl
Innerchr1:206712713..206748442hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3835730
hg1935730
hg1835730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv736031
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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