A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899974



Internal ID15847244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47685552..47688321hg38UCSC Ensembl
Innerchr19:48188809..48191578hg19UCSC Ensembl
Innerchr19:52880621..52883390hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382770
hg192770
hg182770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579889
Supporting Variants
Samples
Known GenesGLTSCR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899974
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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