A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902197



Internal ID22677352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71423974..71427695hg38UCSC Ensembl
chr4:72289691..72293412hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg383722
hg193722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419132
Samples
Known GenesSLC4A4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902197
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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