A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3205



Internal ID15537933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:146664151..146678695hg38UCSC Ensembl
Outerchr3:146381938..146396482hg19UCSC Ensembl
Outerchr3:147864628..147879172hg18UCSC Ensembl
Outerchr3:147864636..147879180hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3814545
hg1914545
hg1814545
hg1714545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4047
Supporting Variants
SamplesNA12878
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)nssv3205
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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