A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155683



Internal ID21457126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146450901..146456468hg38UCSC Ensembl
chr6:146772037..146777604hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg385568
hg195568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581009
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155683
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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