A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528059



Internal ID20901420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75248469..75250762hg38UCSC Ensembl
chr17:73244550..73246843hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382294
hg192294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037508
Samples
Known GenesGGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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