A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453149



Internal ID22511022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46028686..46056595hg38UCSC Ensembl
chr10:51539227..51567136hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3827910
hg1927910
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858850
Supporting Variants
Samples
Known GenesMSMB, NCOA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453149
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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