A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444292



Internal ID222669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156788033..156788144hg38UCSC Ensembl
chr3:156505822..156505933hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940053
Samples
Known GenesLINC00886
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444292
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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