A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616146



Internal ID20989217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152905617..152906604hg38UCSC Ensembl
chr6:153226752..153227739hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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