A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008604



Internal ID20575645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38352501..38353700hg38UCSC Ensembl
chr13:38926638..38927837hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491552
Supporting Variants
Samples
Known GenesUFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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