A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026121



Internal ID20593161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61847206..61848785hg38UCSC Ensembl
chr15:62139405..62140984hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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