A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369295



Internal ID22594964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100735524..100735593hg38UCSC Ensembl
chr13:101387778..101387847hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946803
Supporting Variants
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369295
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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