A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153442



Internal ID21475412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9761898..9765894hg38UCSC Ensembl
chr6:9762131..9766127hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg383997
hg193997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576492
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153442
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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