A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010830



Internal ID20577870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61425716..61426236hg38UCSC Ensembl
chr13:61999849..62000369hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478937
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010830
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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