A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408883



Internal ID21066436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6453646..6457482hg38UCSC Ensembl
chr6:6453879..6457715hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383837
hg193837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143578
Samples
Known GenesLY86-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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