A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530158



Internal ID20903519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82593226..82636244hg38UCSC Ensembl
chr17:80551102..80594120hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3843019
hg1943019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038318
Samples
Known GenesFOXK2, WDR45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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