A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3915



Internal ID15548572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99173824..99221209hg38UCSC Ensembl
Outerchr3:98892668..98940053hg19UCSC Ensembl
Outerchr3:100375358..100422743hg18UCSC Ensembl
Outerchr3:100375358..100422743hg17UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3847386
hg1947386
hg1847386
hg1747386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7837, nssv3184
SamplesNA12156, NA12878
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)nsv3915
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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