A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477152



Internal ID21134705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82769974..82770513hg38UCSC Ensembl
chr13:83344109..83344648hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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