A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6567



Internal ID15537296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:34633087..34655559hg38UCSC Ensembl
Outerchr1:35098688..35121160hg19UCSC Ensembl
Outerchr1:34871275..34893747hg18UCSC Ensembl
Outerchr1:34767781..34790253hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3822473
hg1922473
hg1822473
hg1722473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv399
Supporting Variants
SamplesNA12156
Known Genes
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)nssv6567
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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