A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026104



Internal ID20593144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61559810..61560310hg38UCSC Ensembl
chr15:61852009..61852509hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514584
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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