A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5392



Internal ID15550197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:90415452..90461047hg38UCSC Ensembl
Outerchr6:91125171..91170766hg19UCSC Ensembl
Outerchr6:91181892..91227487hg18UCSC Ensembl
Outerchr6:91181892..91227487hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3845596
hg1945596
hg1845596
hg1745596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6079
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)nsv5392
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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