A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393444



Internal ID21050997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133860650..133861001hg38UCSC Ensembl
chr4:134781805..134782156hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109411
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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