A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546605



Internal ID21870960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73446620..73446682hg38UCSC Ensembl
chr4:74312337..74312399hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998342
Supporting Variants
Samples
Known GenesAFP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546605
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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