A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5173



Internal ID15549956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:1144919..1190408hg38UCSC Ensembl
Outerchr6:1145154..1190643hg19UCSC Ensembl
Outerchr6:1090154..1135643hg18UCSC Ensembl
Outerchr6:1090154..1135643hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3845490
hg1945490
hg1845490
hg1745490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6048
SamplesNA12156
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)nsv5173
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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