A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485501



Internal ID22543412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42510244..42511757hg38UCSC Ensembl
chr2:42737384..42738897hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832670
Supporting Variants
Samples
Known GenesMTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485501
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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