A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1664



Internal ID15545401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:26382348..26406839hg38UCSC Ensembl
Outerchr3:26423839..26448330hg19UCSC Ensembl
Outerchr3:26398843..26423334hg18UCSC Ensembl
Outerchr3:26398843..26423334hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3824492
hg1924492
hg1824492
hg1724492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3741
Supporting Variants
SamplesNA19240
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)nssv1664
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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