A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382024



Internal ID21039577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55554546..55558333hg38UCSC Ensembl
chr4:56420713..56424500hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383788
hg193788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118370
Samples
Known GenesPDCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382024
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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