A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006758



Internal ID20573798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100762681..100775510hg38UCSC Ensembl
chr13:101414935..101427764hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3812830
hg1912830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484452
Supporting Variants
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006758
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