A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6010



Internal ID15537854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:84640927..84662438hg38UCSC Ensembl
Outerchr5:83936745..83958256hg19UCSC Ensembl
Outerchr5:83972501..83994012hg18UCSC Ensembl
Outerchr5:83972501..83994012hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3821512
hg1921512
hg1821512
hg1721512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4907
Supporting Variants
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)nssv6010
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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