A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1926n209



Internal ID22828001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142637379..142797453hg38UCSC Ensembl
chr7:142344882..142495137hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38160075
hg19150256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5912414, nsv5918547, nsv5925755, nsv5909140
Samples
Known GenesMTRNR2L6, PRSS1, PRSS2, PRSS3P2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1926n209
Frequency
Sample Size914
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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