A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4701



Internal ID15196323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:186860797..186883021hg38UCSC Ensembl
Outerchr3:186578586..186600810hg19UCSC Ensembl
Outerchr3:188061280..188083504hg18UCSC Ensembl
Outerchr3:188061288..188083512hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3822225
hg1922225
hg1822225
hg1722225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4155
Supporting Variants
SamplesNA19129
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)nssv4701
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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