A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427385



Internal ID22485255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51897419..51902841hg38UCSC Ensembl
chr3:51931435..51936857hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg385423
hg195423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900070
Supporting Variants
Samples
Known GenesIQCF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427385
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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