A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578816



Internal ID16019539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20388716..20588017hg38UCSC Ensembl
Innerchr19:20499525..20770823hg19UCSC Ensembl
Innerchr19:20360525..20562663hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38199302
hg19271299
hg18202139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6304n54
Supporting Variantsnssv1149855
SamplesHGDP01237
Known GenesMIR1270-1, MIR1270-2, ZNF737, ZNF826P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578816
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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