A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888866



Internal ID22663876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156395245..156395580hg38UCSC Ensembl
chr3:156113034..156113369hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415865
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888866
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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