A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476091



Internal ID253711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32704121..32772242hg38UCSC Ensembl
chr7:32743733..32811854hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3868122
hg1968122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16996070
Samples
Known GenesDPY19L1P1, LINC00997, MIR550A2, MIR550B2, ZNRF2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476091
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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