A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548098



Internal ID16335507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166625972..166653943hg38UCSC Ensembl
Innerchr1:166595209..166623180hg19UCSC Ensembl
Innerchr1:164861833..164889804hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3827972
hg1927972
hg1827972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv727725
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548098
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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