A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408159



Internal ID21065712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79254214..79258020hg38UCSC Ensembl
chr5:78550037..78553843hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg383807
hg193807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133417
Samples
Known GenesJMY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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