A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5197



Internal ID15549982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:10825297..10870387hg38UCSC Ensembl
Outerchr6:10825530..10870620hg19UCSC Ensembl
Outerchr6:10933516..10978606hg18UCSC Ensembl
Outerchr6:10933516..10978606hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3845091
hg1945091
hg1845091
hg1745091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8222
SamplesNA12156
Known GenesMAK
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)nsv5197
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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