A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4911



Internal ID15549668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:87976496..88008395hg38UCSC Ensembl
Outerchr5:87272313..87304212hg19UCSC Ensembl
Outerchr5:87308069..87339968hg18UCSC Ensembl
Outerchr5:87308069..87339968hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3831900
hg1931900
hg1831900
hg1731900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2530
SamplesNA18555
Known Genes
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)nsv4911
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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