A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422470



Internal ID22480340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43985513..43985571hg38UCSC Ensembl
chr4:43987530..43987588hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422470
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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