A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396518



Internal ID21054071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74699901..74701400hg38UCSC Ensembl
chr6:75409617..75411116hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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