A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457578



Internal ID22515459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61933171..61937601hg38UCSC Ensembl
chr10:63692930..63697360hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg384431
hg194431
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856331
Supporting Variants
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457578
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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