A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2534



Internal ID15540587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:97058895..97091636hg38UCSC Ensembl
Outerchr5:96394599..96427340hg19UCSC Ensembl
Outerchr5:96420355..96453096hg18UCSC Ensembl
Outerchr5:96420355..96453096hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg387290
hg197290
hg187290
hg177290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4925
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)nssv2534
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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