A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10782



Internal ID15542016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122600633..122639333hg38UCSC Ensembl
Outerchr10:124360149..124398849hg19UCSC Ensembl
Outerchr10:124350139..124388839hg18UCSC Ensembl
Outerchr10:124350139..124388839hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3838701
hg1938701
hg1838701
hg1738701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7581
Supporting Variants
SamplesNA18956
Known GenesDMBT1
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)nssv10782
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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