A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124065



Internal ID21418813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175788637..175788713hg38UCSC Ensembl
chr5:175215640..175215716hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575170
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124065
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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