A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386352



Internal ID21043905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88006601..88008600hg38UCSC Ensembl
chr4:88927753..88929752hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121805
Samples
Known GenesPKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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