A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8778



Internal ID15535086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69102246..69146941hg38UCSC Ensembl
Outerchr10:70862002..70906697hg19UCSC Ensembl
Outerchr10:70532008..70576703hg18UCSC Ensembl
Outerchr10:70532008..70576703hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3844696
hg1944696
hg1844696
hg1744696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7010
Supporting Variants
SamplesNA12156
Known GenesSRGN, VPS26A
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)nssv8778
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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