A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512



Internal ID15538240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:24987838..25031975hg38UCSC Ensembl
Outerchr7:25027457..25071594hg19UCSC Ensembl
Outerchr7:24993982..25038119hg18UCSC Ensembl
Outerchr7:24800697..24844834hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3844138
hg1944138
hg1844138
hg1744138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5668
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)nssv3512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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