A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608219



Internal ID20981290
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 StatusM
Merged Variants
Supporting Variantsnssv18158714
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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