A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385375



Internal ID22443245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74968254..74968254hg38UCSC Ensembl
chr14:75434957..75434957hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385375
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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