A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488252



Internal ID21145805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51809690..51810438hg38UCSC Ensembl
chr13:52383826..52384574hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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