A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390008



Internal ID21047561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124667601..124668500hg38UCSC Ensembl
chr4:125588756..125589655hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109821
Samples
Known GenesANKRD50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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