A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382494



Internal ID21040047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94597789..94598350hg38UCSC Ensembl
chr4:95518940..95519501hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120776
Samples
Known GenesPDLIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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