A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399192



Internal ID21056745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12139204..12142261hg38UCSC Ensembl
chr6:12139437..12142494hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg383058
hg193058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137540
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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