A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491988



Internal ID269214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86806779..86828779hg38UCSC Ensembl
chr7:86436095..86458095hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999547
Samples
Known GenesGRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491988
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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