A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4982



Internal ID15544051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56569528..56591647hg38UCSC Ensembl
Outerchr7:56637221..56659340hg19UCSC Ensembl
Outerchr7:56604715..56626834hg18UCSC Ensembl
Outerchr7:56411430..56433549hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3822120
hg1922120
hg1822120
hg1722120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5758
Supporting Variants
SamplesNA19129
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)nssv4982
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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