A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423091



Internal ID22480961
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 StatusS
Merged Variantsnsv5897461
Supporting Variants
Samples
Known GenesELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423091
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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