A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7483



Internal ID15205811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:87227293..87405077hg38UCSC Ensembl
Outerchr10:88987050..89164834hg19UCSC Ensembl
Outerchr10:88977030..89154814hg18UCSC Ensembl
Outerchr10:88977030..89154814hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38177785
hg19177785
hg18177785
hg17177785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10771, nssv956, nssv5302
SamplesNA18956, NA19240, NA19129
Known GenesLINC00864, LOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
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)nsv7483
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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