A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378005



Internal ID21035558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135686329..135698237hg38UCSC Ensembl
chr4:136607484..136619392hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3811909
hg1911909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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