A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213771



Internal ID20780811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164109723..164171825hg38UCSC Ensembl
chr4:165030875..165092977hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3862103
hg1962103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385876
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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