A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367917



Internal ID21025470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143574839..143575367hg38UCSC Ensembl
chr3:143293681..143294209hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094410
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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