A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892091



Internal ID16186047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2701508..2702133hg38UCSC Ensembl
Innerchr19:2701506..2702131hg19UCSC Ensembl
Innerchr19:2652506..2653131hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38626
hg19626
hg18626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578391
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)nssv892091
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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