A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294780



Internal ID20503998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38144170..38144227hg38UCSC Ensembl
chr6:38111946..38112003hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731819
Supporting Variants
Samples
Known GenesZFAND3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294780
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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