A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381426



Internal ID21038979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119338985..119570858hg38UCSC Ensembl
chr4:120260140..120492013hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38231874
hg19231874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108940
Samples
Known GenesLINC01061, LOC645513, PDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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