A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125438



Internal ID21452650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173471015..173471078hg38UCSC Ensembl
chr5:172898018..172898081hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575021
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125438
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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