A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123483



Internal ID21418971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182124895..182124955hg38UCSC Ensembl
chr4:183046048..183046108hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574817
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123483
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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