A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578588



Internal ID16365997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9165490..9175919hg38UCSC Ensembl
Innerchr19:9276166..9286595hg19UCSC Ensembl
Innerchr19:9137166..9147595hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810430
hg1910430
hg1810430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6263n54
Supporting Variantsnssv893490, nssv893489
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578588
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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