A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286934



Internal ID20496152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31510487..31511102hg38UCSC Ensembl
chr15:31802690..31803305hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742440
Supporting Variants
Samples
Known GenesOTUD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286934
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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