A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2668



Internal ID15540440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:80098969..80131381hg38UCSC Ensembl
Outerchr7:79728285..79760697hg19UCSC Ensembl
Outerchr7:79566221..79598633hg18UCSC Ensembl
Outerchr7:79372936..79405348hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg387588
hg197588
hg187588
hg177588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5810
Supporting Variants
SamplesNA18555
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)nssv2668
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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