A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366325



Internal ID21023878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143647346..143661884hg38UCSC Ensembl
chr3:143366188..143380726hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3814539
hg1914539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209673
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366325
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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