A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419481



Internal ID22477351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84624346..84625897hg38UCSC Ensembl
chr4:85545499..85547050hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899598
Supporting Variants
Samples
Known GenesCDS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419481
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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