A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4961



Internal ID15549723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:113610211..113655455hg38UCSC Ensembl
Outerchr5:112945908..112991152hg19UCSC Ensembl
Outerchr5:112973807..113019051hg18UCSC Ensembl
Outerchr5:112973807..113019051hg17UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3845245
hg1945245
hg1845245
hg1745245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8136
SamplesNA12156
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)nsv4961
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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