A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048625



Internal ID20615665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57472029..57472682hg38UCSC Ensembl
chr19:57983397..57984050hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530878
Supporting Variants
Samples
Known GenesZNF772
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer