A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3910



Internal ID15191951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132350184..132372201hg38UCSC Ensembl
Outerchr10:134163688..134185705hg19UCSC Ensembl
Outerchr10:134013678..134035695hg18UCSC Ensembl
Outerchr10:134013678..134035695hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg388185
hg198185
hg188185
hg178185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7627
Supporting Variants
SamplesNA12878
Known GenesLRRC27
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)nssv3910
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