A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8765



Internal ID15535099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:22506015..22551071hg38UCSC Ensembl
Outerchr1:22832508..22877564hg19UCSC Ensembl
Outerchr1:22705095..22750151hg18UCSC Ensembl
Outerchr1:22577814..22622870hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3845057
hg1945057
hg1845057
hg1745057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6298
Supporting Variants
SamplesNA12156
Known GenesZBTB40
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)nssv8765
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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