A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396338



Internal ID21053891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90120899..90125151hg38UCSC Ensembl
chr6:90830618..90834870hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384253
hg194253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145370
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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