A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024603



Internal ID20591643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45198683..45200384hg38UCSC Ensembl
chr15:45490881..45492582hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499453
Supporting Variants
Samples
Known GenesSHF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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