A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271808



Internal ID20481026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94625448..94625529hg38UCSC Ensembl
chr5:93961153..93961234hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735127
Supporting Variants
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271808
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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