A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462496



Internal ID22520381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17186092..17187691hg38UCSC Ensembl
chr10:17228091..17229690hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848735
Supporting Variants
Samples
Known GenesTRDMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462496
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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