A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045516



Internal ID20612556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20387257..20790160hg38UCSC Ensembl
chr19:20498066..20972966hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38402904
hg19474901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517053
Supporting Variants
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF626, ZNF737, ZNF826P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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