A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526



Internal ID15550344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:147822855..147882121hg38UCSC Ensembl
Outerchr6:148143991..148203257hg19UCSC Ensembl
Outerchr6:148185684..148244950hg18UCSC Ensembl
Outerchr6:148185684..148244950hg17UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg387980
hg197980
hg187980
hg177980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10520, nssv6094
SamplesNA12156, NA18956
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)nsv5526
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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