A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375688



Internal ID21033241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128117521..128120556hg38UCSC Ensembl
chr4:129038676..129041711hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg383036
hg193036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110504
Samples
Known GenesLARP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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