A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546631



Internal ID16334040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79053125..79149304hg38UCSC Ensembl
Innerchr1:79518810..79614989hg19UCSC Ensembl
Innerchr1:79291398..79387577hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3896180
hg1996180
hg1896180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv717746
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546631
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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