A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199000



Internal ID20766040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6950799..7124736hg38UCSC Ensembl
chr19:6950810..7124747hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38173938
hg19173938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521542
Supporting Variants
Samples
Known GenesEMR4P, FLJ25758, INSR, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199000
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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