A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146560



Internal ID20713600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56776001..56780200hg38UCSC Ensembl
chr6:56640799..56644998hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411692
Supporting Variants
Samples
Known GenesDST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00206


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