A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5779



Internal ID15550622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:67784777..67817684hg38UCSC Ensembl
Outerchr7:67249764..67282671hg19UCSC Ensembl
Outerchr7:66887199..66920106hg18UCSC Ensembl
Outerchr7:66693914..66726821hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg386380
hg196380
hg186380
hg176380
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4990
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)nsv5779
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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