A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899601



Internal ID16193557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42046231..42047637hg38UCSC Ensembl
Innerchr19:42550383..42551789hg19UCSC Ensembl
Innerchr19:47242223..47243629hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381407
hg191407
hg181407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579629
Supporting Variants
Samples
Known GenesGRIK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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