A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892916



Internal ID16186872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4065794..4069428hg38UCSC Ensembl
Innerchr19:4065792..4069426hg19UCSC Ensembl
Innerchr19:4016792..4020426hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383635
hg193635
hg183635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578441
Supporting Variants
Samples
Known GenesZBTB7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892916
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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