A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389490



Internal ID21047043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112258370..112258805hg38UCSC Ensembl
chr4:113179526..113179961hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105617
Samples
Known GenesAP1AR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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