A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897461



Internal ID22672564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139061224..139062219hg38UCSC Ensembl
chr4:139982378..139983373hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38996
hg19996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423091
Samples
Known GenesELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897461
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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