A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611733



Internal ID20984804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22318458..22318968hg38UCSC Ensembl
chr7:22358077..22358587hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154244
Samples
Known GenesRAPGEF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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