A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608854



Internal ID20981925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122328229..122330851hg38UCSC Ensembl
chr7:121968283..121970905hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg382623
hg192623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151864
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608854
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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