A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391081



Internal ID21048634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164543299..164814465hg38UCSC Ensembl
chr4:165464451..165735617hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38271167
hg19271167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114502
Samples
Known GenesLOC100505989, MIR5684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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