A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546015



Internal ID16333424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37169903..37235080hg38UCSC Ensembl
Innerchr1:37635504..37700681hg19UCSC Ensembl
Innerchr1:37408091..37473268hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3865178
hg1965178
hg1865178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv234n54
Supporting Variantsnssv712362
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546015
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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