A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546014



Internal ID16333423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37169903..37218318hg38UCSC Ensembl
Innerchr1:37635504..37683919hg19UCSC Ensembl
Innerchr1:37408091..37456506hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3848416
hg1948416
hg1848416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv233n54
Supporting Variantsnssv712361
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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