A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901322



Internal ID15848592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54053325..54055338hg38UCSC Ensembl
Innerchr19:54556579..54558592hg19UCSC Ensembl
Innerchr19:59248391..59250404hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382014
hg192014
hg182014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580127
Supporting Variants
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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