A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158714



Internal ID20725754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:715012..717075hg38UCSC Ensembl
chr7:754649..756712hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382064
hg192064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608219
Supporting Variants
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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