A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433195



Internal ID21090748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141713378..141715536hg38UCSC Ensembl
chr7:141413178..141415336hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150779
Samples
Known GenesWEE2, WEE2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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