A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569



Internal ID15538297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:113770630..113797317hg38UCSC Ensembl
Outerchr7:113410685..113437372hg19UCSC Ensembl
Outerchr7:113197921..113224608hg18UCSC Ensembl
Outerchr7:113004636..113031323hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3826688
hg1926688
hg1826688
hg1726688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911
Supporting Variants
SamplesNA12878
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)nssv3569
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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