A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145855



Internal ID21476071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77042480..77042671hg38UCSC Ensembl
chr5:76338305..76338496hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580763
Supporting Variants
SamplesHG03486
Known GenesAGGF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145855
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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