A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407061



Internal ID21064614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80345994..80351014hg38UCSC Ensembl
chr5:79641813..79646833hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg385021
hg195021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133486
Samples
Known GenesCRSP8P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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