A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613555



Internal ID20986626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99476056..99485112hg38UCSC Ensembl
chr6:99923932..99932988hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg389057
hg199057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147638
Samples
Known GenesUSP45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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