A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127526



Internal ID21497603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51535607..51535607hg38UCSC Ensembl
chr5:50831441..50831441hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634891
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127526
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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