A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891499



Internal ID15838769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049570..1049830hg38UCSC Ensembl
Innerchr19:1049569..1049829hg19UCSC Ensembl
Innerchr19:1000569..1000829hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38261
hg19261
hg18261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578205
Supporting Variants
Samples
Known GenesABCA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891499
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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