A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451996



Internal ID22509868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114398972..114401271hg38UCSC Ensembl
chr10:116158731..116161030hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855705
Supporting Variants
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451996
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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