A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144676



Internal ID21465588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124847965..124849328hg38UCSC Ensembl
chr6:125169111..125170474hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578254
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144676
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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