A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6111



Internal ID15537752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1194152..1198971hg38UCSC Ensembl
Outerchr7:1233788..1238607hg19UCSC Ensembl
Outerchr7:1200314..1205133hg18UCSC Ensembl
Outerchr7:1007029..1011848hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3810280
hg1910280
hg1810280
hg1710280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613
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)nssv6111
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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