A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548073



Internal ID15988796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161605657..161661908hg38UCSC Ensembl
Innerchr1:161575447..161631698hg19UCSC Ensembl
Innerchr1:159842071..159898322hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3856252
hg1956252
hg1856252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv607n54
Supporting Variantsnssv727699
Samples
Known GenesFCGR3B, HSPA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548073
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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