A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5781



Internal ID15550625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:69056710..69089140hg38UCSC Ensembl
Outerchr7:68521697..68554127hg19UCSC Ensembl
Outerchr7:68159633..68192063hg18UCSC Ensembl
Outerchr7:67966348..67998778hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg386952
hg196952
hg186952
hg176952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6139
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)nsv5781
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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