A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3865



Internal ID15538592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8833059..8867232hg38UCSC Ensembl
Outerchr10:8875022..8909195hg19UCSC Ensembl
Outerchr10:8915028..8949201hg18UCSC Ensembl
Outerchr10:8915028..8949201hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385570
hg195570
hg185570
hg175570
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5776
Supporting Variants
SamplesNA12878
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)nssv3865
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