A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137849



Internal ID21446134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1857815..1857865hg38UCSC Ensembl
chr5:1857929..1857979hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577886
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137849
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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