A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545722



Internal ID16333131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:19056197..19060848hg38UCSC Ensembl
Innerchr1:19382691..19387342hg19UCSC Ensembl
Innerchr1:19255278..19259929hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384652
hg194652
hg184652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711252
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545722
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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