A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516615



Internal ID20889976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59039527..59137081hg38UCSC Ensembl
chr17:57116888..57214442hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3897555
hg1997555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036344
Samples
Known GenesSKA2, TRIM37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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