A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891570



Internal ID15838840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049726..1049882hg38UCSC Ensembl
Innerchr19:1049725..1049881hg19UCSC Ensembl
Innerchr19:1000725..1000881hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38157
hg19157
hg18157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578210
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)nssv891570
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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