A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023944



Internal ID20590984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42550721..42558599hg38UCSC Ensembl
chr15:42842919..42850797hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg387879
hg197879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498158
Supporting Variants
Samples
Known GenesHAUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023944
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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