A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396353



Internal ID21053906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25780730..25782758hg38UCSC Ensembl
chr6:25780958..25782986hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg382029
hg192029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140710
Samples
Known GenesSLC17A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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