A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891375



Internal ID15838645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049519..1049777hg38UCSC Ensembl
Innerchr19:1049518..1049776hg19UCSC Ensembl
Innerchr19:1000518..1000776hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38259
hg19259
hg18259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578197
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)nssv891375
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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