A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014566



Internal ID20581606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87835082..87837219hg38UCSC Ensembl
chr13:88487337..88489474hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg382138
hg192138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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