A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487996



Internal ID21145549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29758797..29759536hg38UCSC Ensembl
chr13:30332934..30333673hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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