A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10537



Internal ID15542261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:20706453..20722919hg38UCSC Ensembl
Outerchr7:20746076..20762542hg19UCSC Ensembl
Outerchr7:20712601..20729067hg18UCSC Ensembl
Outerchr7:20519316..20535782hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3816467
hg1916467
hg1816467
hg1716467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5651
Supporting Variants
SamplesNA18956
Known GenesABCB5
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)nssv10537
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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