A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443731



Internal ID22501601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:651487..651588hg38UCSC Ensembl
chr7:691124..691225hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918417
Supporting Variants
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443731
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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