A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444006



Internal ID21101559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77915138..77923830hg38UCSC Ensembl
chr10:79674896..79683588hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg388693
hg198693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984348
Samples
Known GenesDLG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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