A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503676



Internal ID280497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100759889..100857140hg38UCSC Ensembl
chr13:101412143..101509394hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3897252
hg1997252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691225
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503676
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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