A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891296



Internal ID15838566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049468..1049936hg38UCSC Ensembl
Innerchr19:1049467..1049935hg19UCSC Ensembl
Innerchr19:1000467..1000935hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38469
hg19469
hg18469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578193
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)nssv891296
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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