A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145413



Internal ID20712453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90685501..90686300hg38UCSC Ensembl
chr6:91395220..91396019hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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