A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617996



Internal ID20991067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153293987..153307443hg38UCSC Ensembl
chr6:153615122..153628578hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3813457
hg1913457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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