A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148761



Internal ID20715801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92618414..92618949hg38UCSC Ensembl
chr6:93328132..93328667hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00078


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