A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521697



Internal ID20895058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51072360..51079441hg38UCSC Ensembl
chr17:49149721..49156802hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg387082
hg197082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036837
Samples
Known GenesSPAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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