A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7631



Internal ID15205974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133388509..133573114hg38UCSC Ensembl
Outerchr10:135202013..135386618hg19UCSC Ensembl
Outerchr10:135052003..135236608hg18UCSC Ensembl
Outerchr10:135090894..135275499hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38184606
hg19184606
hg18184606
hg17184606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976, nssv8872
SamplesNA12156, NA19240
Known GenesCYP2E1, MTG1, PAOX, SCART1, SPRN, SPRNP1, SYCE1
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)nsv7631
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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