A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8393



Internal ID15535471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:84489671..84523080hg38UCSC Ensembl
Outerchr7:84118987..84152396hg19UCSC Ensembl
Outerchr7:83956923..83990332hg18UCSC Ensembl
Outerchr7:83763638..83797047hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg386026
hg196026
hg186026
hg176026
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5819
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)nssv8393
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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