A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4932



Internal ID15542898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:85974323..86012669hg38UCSC Ensembl
Outerchr6:86684041..86722387hg19UCSC Ensembl
Outerchr6:86740760..86779106hg18UCSC Ensembl
Outerchr6:86740760..86779106hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3838347
hg1938347
hg1838347
hg1738347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5384
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)nssv4932
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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