A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578393



Internal ID16365802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2701508..2702242hg38UCSC Ensembl
Innerchr19:2701506..2702240hg19UCSC Ensembl
Innerchr19:2652506..2653240hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38735
hg19735
hg18735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6220n54
Supporting Variantsnssv892093, nssv892094
Samples
Known GenesGNG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578393
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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