A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5370



Internal ID15203487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:80005634..80042023hg38UCSC Ensembl
Outerchr6:80715351..80751740hg19UCSC Ensembl
Outerchr6:80772070..80808459hg18UCSC Ensembl
Outerchr6:80772070..80808459hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3836390
hg1936390
hg1836390
hg1736390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8267
SamplesNA12156
Known GenesTTK
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)nsv5370
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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