A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397522



Internal ID21055075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87716501..87717800hg38UCSC Ensembl
chr6:88426219..88427518hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397522
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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