A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579422



Internal ID16020145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35665686..35774606hg38UCSC Ensembl
Innerchr19:36156588..36265508hg19UCSC Ensembl
Innerchr19:40848428..40957348hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38108921
hg19108921
hg18108921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898982
Samples
Known GenesC19orf55, HSPB6, IGFLR1, KMT2B, LIN37, PSENEN, U2AF1L4, UPK1A, UPK1A-AS1, ZBTB32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579422
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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