A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7517



Internal ID15552534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:99913088..99914337hg38UCSC Ensembl
Outerchr10:101672845..101674094hg19UCSC Ensembl
Outerchr10:101662835..101664084hg18UCSC Ensembl
Outerchr10:101662835..101664084hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384607
hg194607
hg184607
hg174607
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3896
SamplesNA12878
Known GenesDNMBP
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)nsv7517
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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