A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146989



Internal ID21487867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74999635..74999635hg38UCSC Ensembl
chr5:74295460..74295460hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640982
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146989
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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