A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296571



Internal ID20505789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121034693..121034851hg38UCSC Ensembl
chr10:122794206..122794364hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733753
Supporting Variants
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296571
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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