A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404829



Internal ID21062382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:125582755..126319109hg38UCSC Ensembl
chr5:124918448..125654801hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38736355
hg19736354
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213170
Samples
Known GenesLOC101927488, LOC102546228
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404829
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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