A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534380



Internal ID20907741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2379318..2594919hg38UCSC Ensembl
chr19:2379316..2594917hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38215602
hg19215602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198542
Samples
Known GenesGADD45B, GNG7, LMNB2, MIR7108, TIMM13, TMPRSS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534380
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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