A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397039



Internal ID21054592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86963997..86964655hg38UCSC Ensembl
chr6:87673715..87674373hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149068
Samples
Known GenesHTR1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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