A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142416



Internal ID21476626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76170754..76173075hg38UCSC Ensembl
chr5:75466579..75468900hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg382322
hg192322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579652
Supporting Variants
SamplesHG03486
Known GenesSV2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142416
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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