A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156527



Internal ID22086928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73344723..73421886hg38UCSC Ensembl
Outerchr6:73340055..73424476hg38UCSC Ensembl
Innerchr6:74054446..74131609hg19UCSC Ensembl
Outerchr6:74049778..74134199hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3884422
hg1984422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019853
Samples
Known GenesDDX43, DPPA5, KHDC3L, OOEP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156527
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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