A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609130



Internal ID20982201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145684308..145685076hg38UCSC Ensembl
chr6:146005444..146006212hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140969
Samples
Known GenesEPM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609130
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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