A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7545



Internal ID15552565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:109802929..109837931hg38UCSC Ensembl
Outerchr10:111562687..111597689hg19UCSC Ensembl
Outerchr10:111552677..111587679hg18UCSC Ensembl
Outerchr10:111552677..111587679hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3835003
hg1935003
hg1835003
hg1735003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5317, nssv1909, nssv10778, nssv965, nssv3898, nssv6416
SamplesNA12156, NA12878, NA18956, NA18555, NA19240, NA19129
Known Genes
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)nsv7545
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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