A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454131



Internal ID22512007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60433019..60436002hg38UCSC Ensembl
chr10:62192777..62195760hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg382984
hg192984
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859374
Supporting Variants
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454131
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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