A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7757n223



Internal ID22810725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63291101..63321700hg38UCSC Ensembl
chr9:67246073..67276672hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3830600
hg1930600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6437555, nsv6447113, nsv6446975
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7757n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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