A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8097



Internal ID15189081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:39095098..39122592hg38UCSC Ensembl
Outerchr5:39095200..39122694hg19UCSC Ensembl
Outerchr5:39130957..39158451hg18UCSC Ensembl
Outerchr5:39130957..39158451hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3827495
hg1927495
hg1827495
hg1727495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4805
Supporting Variants
SamplesNA12156
Known GenesFYB
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)nssv8097
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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