A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615322



Internal ID20988393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122839299..122841183hg38UCSC Ensembl
chr7:122479353..122481237hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg381885
hg191885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149409
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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