A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4943



Internal ID15542881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:132990526..133035561hg38UCSC Ensembl
Outerchr6:133311665..133356700hg19UCSC Ensembl
Outerchr6:133353358..133398393hg18UCSC Ensembl
Outerchr6:133353358..133398393hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3845036
hg1945036
hg1845036
hg1745036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481
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)nssv4943
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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