A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018314



Internal ID22079945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:11074069..11076965hg38UCSC Ensembl
Outerchr6:11071891..11084404hg38UCSC Ensembl
Innerchr6:11074302..11077198hg19UCSC Ensembl
Outerchr6:11072124..11084637hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3812514
hg1912514
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156459
Supporting Variants
Samples
Known GenesELOVL2-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018314
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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