A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524813



Internal ID20898174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25647327..25674465hg38UCSC Ensembl
chr20:25627963..25655101hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3827139
hg1927139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067181
Samples
Known GenesZNF337
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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