A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7515



Internal ID15205846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:99606658..99639439hg38UCSC Ensembl
Outerchr10:101366415..101399196hg19UCSC Ensembl
Outerchr10:101356405..101389186hg18UCSC Ensembl
Outerchr10:101356405..101389186hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg388222
hg198222
hg188222
hg178222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv961
SamplesNA19240
Known GenesSLC25A28
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)nsv7515
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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