A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1909n209



Internal ID22827984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76448810..76997234hg38UCSC Ensembl
chr7:76078127..76626551hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38548425
hg19548425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5924813, nsv5922377, nsv5917718
Samples
Known GenesDTX2, DTX2P1-UPK3BP1-PMS2P11, FDPSP2, LOC100133091, POMZP3, UPK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1909n209
Frequency
Sample Size914
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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