A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10676



Internal ID15195436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15109726..15140827hg38UCSC Ensembl
Outerchr10:15151725..15182826hg19UCSC Ensembl
Outerchr10:15191731..15222832hg18UCSC Ensembl
Outerchr10:15191731..15222832hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg388398
hg198398
hg188398
hg178398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910
Supporting Variants
SamplesNA18956
Known GenesNMT2
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)nssv10676
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