A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6559



Internal ID15537304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:50489137..50513083hg38UCSC Ensembl
Outerchr13:51063273..51087219hg19UCSC Ensembl
Outerchr13:49961274..49985220hg18UCSC Ensembl
Outerchr13:49961274..49985220hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3823947
hg1923947
hg1823947
hg1723947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040
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)nssv6559
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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