A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5308



Internal ID15543358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98921448..98964725hg38UCSC Ensembl
Outerchr10:100681205..100724482hg19UCSC Ensembl
Outerchr10:100671195..100714472hg18UCSC Ensembl
Outerchr10:100671195..100714472hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3843278
hg1943278
hg1843278
hg1743278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7513
Supporting Variants
SamplesNA19129
Known GenesHPSE2
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)nssv5308
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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