A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411936



Internal ID22469806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155181452..155187103hg38UCSC Ensembl
chr4:156102604..156108255hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385652
hg195652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411936
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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