A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513111



Internal ID20886451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40217253..40223655hg38UCSC Ensembl
chr17:38373505..38379907hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg386403
hg196403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036021
Samples
Known GenesWIPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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