A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139586



Internal ID21451258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148923221..148923221hg38UCSC Ensembl
chr5:148302784..148302784hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642441
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139586
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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