A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736



Internal ID15549475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:16393846..16438946hg38UCSC Ensembl
Outerchr5:16393955..16439055hg19UCSC Ensembl
Outerchr5:16446955..16492055hg18UCSC Ensembl
Outerchr5:16446955..16492055hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3845101
hg1945101
hg1845101
hg1745101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8074
SamplesNA12156
Known GenesLOC101929505
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)nsv4736
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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