A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3846



Internal ID15548496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:60768511..60813795hg38UCSC Ensembl
Outerchr3:60754244..60799500hg19UCSC Ensembl
Outerchr3:60729284..60774540hg18UCSC Ensembl
Outerchr3:60729284..60774540hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3845285
hg1945257
hg1845257
hg1745257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7813
SamplesNA12156
Known GenesFHIT
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)nsv3846
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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