A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7495



Internal ID15552510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93921932..93987040hg38UCSC Ensembl
Outerchr10:95681689..95746797hg19UCSC Ensembl
Outerchr10:95671679..95736787hg18UCSC Ensembl
Outerchr10:95671679..95736787hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386050
hg196050
hg186050
hg176050
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8830, nssv10773
SamplesNA12156, NA18956
Known GenesPIPSL
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)nsv7495
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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