A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339958



Internal ID20997511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219236393..219237413hg38UCSC Ensembl
chr2:220101115..220102135hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085506
Samples
Known GenesANKZF1, GLB1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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