A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7811



Internal ID15189367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:58544654..58564972hg38UCSC Ensembl
Outerchr3:58530381..58550699hg19UCSC Ensembl
Outerchr3:58505421..58525739hg18UCSC Ensembl
Outerchr3:58505421..58525739hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3820319
hg1920319
hg1820319
hg1720319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3839
Supporting Variants
SamplesNA12156
Known GenesFAM107A
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)nssv7811
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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