A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399085



Internal ID21056638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65200833..65201347hg38UCSC Ensembl
chr5:64496660..64497174hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134397
Samples
Known GenesADAMTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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