A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530501



Internal ID20903862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9566401..9566726hg38UCSC Ensembl
chr20:9547048..9547373hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069237
Samples
Known GenesPAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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