A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545723



Internal ID16333132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:19056197..19068230hg38UCSC Ensembl
Innerchr1:19382691..19394724hg19UCSC Ensembl
Innerchr1:19255278..19267311hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3812034
hg1912034
hg1812034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711253
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545723
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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