A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476560



Internal ID21134113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75933963..75934587hg38UCSC Ensembl
chr13:76508099..76508723hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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