A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150337



Internal ID15872752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14695350..14735523hg38UCSC Ensembl
Innerchr19:14806162..14846335hg19UCSC Ensembl
Innerchr19:14667162..14707335hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3840174
hg1940174
hg1840174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578680
Supporting Variants
SamplesHGDP00029
Known GenesEMR2, ZNF333
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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