A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399253



Internal ID21056806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36398021..36398304hg38UCSC Ensembl
chr6:36365798..36366081hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143225
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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