A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9341



Internal ID15193606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54215005..54270671hg38UCSC Ensembl
Outerchr19:54718874..54774525hg19UCSC Ensembl
Outerchr19:59410686..59466337hg18UCSC Ensembl
Outerchr19:59410686..59466337hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3855667
hg1955652
hg1855652
hg1755652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2546
Supporting Variants
SamplesNA18517
Known GenesLILRA6, LILRB3, LILRB5
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9341
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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