A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494044



Internal ID22551974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65058312..65077818hg38UCSC Ensembl
chr3:65043987..65063493hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3819507
hg1919507
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494044
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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