A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8348



Internal ID15535516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:25650385..25665001hg38UCSC Ensembl
Outerchr7:25690005..25704621hg19UCSC Ensembl
Outerchr7:25656530..25671146hg18UCSC Ensembl
Outerchr7:25463245..25477861hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3814617
hg1914617
hg1814617
hg1714617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670
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)nssv8348
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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