A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3886



Internal ID15191927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:78985313..79019009hg38UCSC Ensembl
Outerchr10:80745070..80778766hg19UCSC Ensembl
Outerchr10:80415076..80448772hg18UCSC Ensembl
Outerchr10:80415076..80448772hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386046
hg196046
hg186046
hg176046
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7343
Supporting Variants
SamplesNA12878
Known GenesZMIZ1-AS1
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)nssv3886
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