A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397690



Internal ID21055243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29460505..29464947hg38UCSC Ensembl
chr6:29428282..29432724hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141361
Samples
Known GenesOR2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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