A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498



Internal ID15203627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:803197..814522hg38UCSC Ensembl
Outerchr10:849137..860462hg19UCSC Ensembl
Outerchr10:839137..850462hg18UCSC Ensembl
Outerchr10:839137..850462hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3811326
hg1911326
hg1811326
hg1711326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8342
SamplesNA12156
Known GenesLARP4B
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)nsv5498
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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