A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494129



Internal ID21151682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73588195..73592821hg38UCSC Ensembl
chr13:74162332..74166958hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg384627
hg194627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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