A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095147



Internal ID21466827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100754385..100764994hg38UCSC Ensembl
chr13:101406639..101417248hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3810610
hg1910610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594649
Supporting Variants
SamplesHG03065
Known GenesNALCN-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095147
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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