A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546016



Internal ID16333425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37169903..37237731hg38UCSC Ensembl
Innerchr1:37635504..37703332hg19UCSC Ensembl
Innerchr1:37408091..37475919hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3867829
hg1967829
hg1867829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv234n54
Supporting Variantsnssv712363
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546016
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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