A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11003



Internal ID15192905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54212629..54265267hg38UCSC Ensembl
Outerchr19:54716498..54769121hg19UCSC Ensembl
Outerchr19:59408310..59460933hg18UCSC Ensembl
Outerchr19:59408310..59460933hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3852639
hg1952624
hg1852624
hg1752624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2546
Supporting Variants
SamplesNA15510
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)nssv11003
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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