A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145113



Internal ID20712153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71402568..71402699hg38UCSC Ensembl
chr6:72112271..72112402hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407333
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00348


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