A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400375



Internal ID21057928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91276401..91410600hg38UCSC Ensembl
chr6:91986119..92120318hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38134200
hg19134200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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