A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910



Internal ID15204081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15109726..15148976hg38UCSC Ensembl
Outerchr10:15151725..15190975hg19UCSC Ensembl
Outerchr10:15191731..15230981hg18UCSC Ensembl
Outerchr10:15191731..15230981hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg388398
hg198398
hg188398
hg178398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10676, nssv5214
SamplesNA18956, NA19129
Known GenesNMT2
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)nsv5910
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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