A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578462



Internal ID16019185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6678457..6679349hg38UCSC Ensembl
Innerchr19:6678468..6679360hg19UCSC Ensembl
Innerchr19:6629468..6630360hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38893
hg19893
hg18893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893184
Samples
Known GenesC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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