A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275749



Internal ID20484967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10435618..10435673hg38UCSC Ensembl
chr5:10435730..10435785hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743427
Supporting Variants
Samples
Known GenesMARCH6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275749
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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