A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4808



Internal ID15549554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:41203152..41251883hg38UCSC Ensembl
Outerchr5:41203254..41251985hg19UCSC Ensembl
Outerchr5:41239011..41287742hg18UCSC Ensembl
Outerchr5:41239011..41287742hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3848732
hg1948732
hg1848732
hg1748732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2519
SamplesNA18555
Known GenesC6
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)nsv4808
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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