A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7837



Internal ID15536027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99176528..99221209hg38UCSC Ensembl
Outerchr3:98895372..98940053hg19UCSC Ensembl
Outerchr3:100378062..100422743hg18UCSC Ensembl
Outerchr3:100378062..100422743hg17UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3844682
hg1944682
hg1844682
hg1744682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3915
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)nssv7837
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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