A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923460



Internal ID22698687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154615583..154615698hg38UCSC Ensembl
chr7:154407293..154407408hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432824
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923460
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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