A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423769



Internal ID22481639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185210390..185210441hg38UCSC Ensembl
chr4:186131544..186131595hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898303
Supporting Variants
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423769
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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