A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999895



Internal ID20566935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20098864..20100922hg38UCSC Ensembl
chr12:20251798..20253856hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg382059
hg192059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469435
Supporting Variants
Samples
Known GenesLOC100506393
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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