A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528948



Internal ID20902309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20386915..21526140hg38UCSC Ensembl
chr19:20497724..21708942hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381139226
hg191211219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198417
Samples
Known GenesLINC00664, MIR1270-1, MIR1270-2, ZNF429, ZNF430, ZNF431, ZNF493, ZNF626, ZNF708, ZNF714, ZNF737, ZNF738, ZNF826P, ZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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