A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606760



Internal ID20979831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:722372..722793hg38UCSC Ensembl
chr7:762009..762430hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158751
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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