A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9263



Internal ID15540214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122599156..122633561hg38UCSC Ensembl
Outerchr10:124358672..124393077hg19UCSC Ensembl
Outerchr10:124348662..124383067hg18UCSC Ensembl
Outerchr10:124348662..124383067hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3834406
hg1934406
hg1834406
hg1734406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7581
Supporting Variants
SamplesNA18517
Known GenesDMBT1
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)nssv9263
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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