A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212017



Internal ID20779057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145605358..145625737hg38UCSC Ensembl
chr4:146526510..146546889hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3820380
hg1920380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394533
Supporting Variants
Samples
Known GenesMMAA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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