A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454253



Internal ID22512129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124808170..124815256hg38UCSC Ensembl
chr10:126496739..126503825hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387087
hg197087
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851601
Supporting Variants
Samples
Known GenesFAM175B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454253
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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