A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511698



Internal ID20885028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40227979..40237403hg38UCSC Ensembl
chr17:38384231..38393655hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg389425
hg199425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036024
Samples
Known GenesWIPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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