A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894855



Internal ID15842125
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 StatusS
Merged Variantsnsv578669
Supporting Variants
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv894855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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