A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513717



Internal ID20887064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52915651..52929935hg38UCSC Ensembl
chr15:53207848..53222132hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3814285
hg1914285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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