A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517053



Internal ID20890414
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 StatusM
Merged Variants
Supporting Variantsnssv18045516
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF626, ZNF737, ZNF826P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517053
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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