A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7493



Internal ID15552508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93034531..93042280hg38UCSC Ensembl
Outerchr10:94794288..94802037hg19UCSC Ensembl
Outerchr10:94784268..94792017hg18UCSC Ensembl
Outerchr10:94784268..94792017hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg387750
hg197750
hg187750
hg177750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4624
SamplesNA19129
Known GenesEXOC6
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)nsv7493
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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