A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383813



Internal ID21041366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122392701..122394300hg38UCSC Ensembl
chr4:123313856..123315455hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109052
Samples
Known GenesADAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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