A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421832



Internal ID22479702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10841865..10841958hg38UCSC Ensembl
chr4:10843489..10843582hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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