A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379762



Internal ID21037315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3177355..3178752hg38UCSC Ensembl
chr5:3177469..3178866hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130899
Samples
Known GenesLOC102467074
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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