A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891783



Internal ID15839053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1371355..1448181hg38UCSC Ensembl
Innerchr19:1371354..1448180hg19UCSC Ensembl
Innerchr19:1322354..1399180hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3876827
hg1976827
hg1876827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578278
Supporting Variants
Samples
Known GenesDAZAP1, GAMT, MUM1, NDUFS7, RPS15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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