A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406631



Internal ID21064184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84212507..84213186hg38UCSC Ensembl
chr6:84922225..84922904hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145961
Samples
Known GenesKIAA1009
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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