A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408329



Internal ID21065882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27814335..27821050hg38UCSC Ensembl
chr6:27782113..27788828hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg386716
hg196716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140833
Samples
Known GenesHIST1H2AJ, HIST1H2BM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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