A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2529



Internal ID15540593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:84649017..84664654hg38UCSC Ensembl
Outerchr5:83944835..83960472hg19UCSC Ensembl
Outerchr5:83980591..83996228hg18UCSC Ensembl
Outerchr5:83980591..83996228hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3815638
hg1915638
hg1815638
hg1715638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4907
Supporting Variants
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)nssv2529
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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