A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411531



Internal ID21069084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56750231..56753727hg38UCSC Ensembl
chr6:56615029..56618525hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146558
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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