A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391079



Internal ID21048632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86713279..86713720hg38UCSC Ensembl
chr4:87634432..87634873hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121740
Samples
Known GenesPTPN13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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