A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9803



Internal ID15539863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98912015..98957764hg38UCSC Ensembl
Outerchr10:100671772..100717521hg19UCSC Ensembl
Outerchr10:100661762..100707511hg18UCSC Ensembl
Outerchr10:100661762..100707511hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3845750
hg1945750
hg1845750
hg1745750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7513
Supporting Variants
SamplesNA18507
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)nssv9803
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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