A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932



Internal ID8517773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:16953295..16998848hg38UCSC Ensembl
Outerchr10:16995294..17040847hg19UCSC Ensembl
Outerchr10:17035300..17080853hg18UCSC Ensembl
Outerchr10:17035300..17080853hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3845554
hg1945554
hg1845554
hg1745554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5239
SamplesNA19129
Known GenesCUBN
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)nsv5932
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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