A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546574



Internal ID16333983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:73808439..73863685hg38UCSC Ensembl
Innerchr1:74274122..74329368hg19UCSC Ensembl
Innerchr1:74046710..74101956hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3855247
hg1955247
hg1855247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv326n54
Supporting Variantsnssv717541
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546574
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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