A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876



Internal ID15550729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101540415..101565638hg38UCSC Ensembl
Outerchr7:101183696..101208918hg19UCSC Ensembl
Outerchr7:100970416..100995638hg18UCSC Ensembl
Outerchr7:100777131..100802353hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389600
hg199600
hg189600
hg179600
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560
SamplesNA12878
Known GenesCOL26A1, LINC01007
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)nsv5876
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