A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561992



Internal ID334958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4775392..4885429hg38UCSC Ensembl
chr7:4815023..4925060hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38110038
hg19110038
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992481
Samples
Known GenesAP5Z1, MIR4656, PAPOLB, RADIL
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561992
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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