A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098234



Internal ID20665274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173002455..173010104hg38UCSC Ensembl
chr3:172720245..172727894hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg387650
hg197650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360273
Supporting Variants
Samples
Known GenesSPATA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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