A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892090



Internal ID16186046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2701508..2701975hg38UCSC Ensembl
Innerchr19:2701506..2701973hg19UCSC Ensembl
Innerchr19:2652506..2652973hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38468
hg19468
hg18468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578390
Supporting Variants
Samples
Known GenesGNG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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