A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5822



Internal ID15550670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:85201137..85211525hg38UCSC Ensembl
Outerchr7:84830453..84840841hg19UCSC Ensembl
Outerchr7:84668389..84678777hg18UCSC Ensembl
Outerchr7:84475104..84485492hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg387172
hg197172
hg187172
hg177172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10563
SamplesNA18956
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)nsv5822
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer