A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377038



Internal ID21034591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135471983..135638834hg38UCSC Ensembl
chr4:136393138..136559989hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38166852
hg19166852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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