A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609096



Internal ID20982167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107136592..107144681hg38UCSC Ensembl
chr7:106777037..106785126hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg388090
hg198090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146938
Samples
Known GenesPRKAR2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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