A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578669



Internal ID16019392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14621589..14622555hg38UCSC Ensembl
Innerchr19:14732401..14733367hg19UCSC Ensembl
Innerchr19:14593401..14594367hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38967
hg19967
hg18967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6280n54
Supporting Variantsnssv894856, nssv894855, nssv894857
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578669
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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