A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575



Internal ID15203712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:161190552..161222447hg38UCSC Ensembl
Outerchr6:161611584..161643479hg19UCSC Ensembl
Outerchr6:161531574..161563469hg18UCSC Ensembl
Outerchr6:161581995..161613890hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3831896
hg1931896
hg1831896
hg1731896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8321
SamplesNA12156
Known GenesAGPAT4
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)nsv5575
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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