A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8872



Internal ID15188306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133484908..133503315hg38UCSC Ensembl
Outerchr10:135298412..135316819hg19UCSC Ensembl
Outerchr10:135148402..135166809hg18UCSC Ensembl
Outerchr10:135187293..135205700hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3818408
hg1918408
hg1818408
hg1718408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7631
Supporting Variants
SamplesNA12156
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)nssv8872
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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