A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405983



Internal ID21063536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91670567..91672631hg38UCSC Ensembl
chr6:92380285..92382349hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382065
hg192065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146150
Samples
Known GenesCASC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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