A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010864



Internal ID20577904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61542186..61580317hg38UCSC Ensembl
chr13:62116319..62154450hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3838132
hg1938132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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