A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533122



Internal ID20906483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58560389..58562427hg38UCSC Ensembl
chr17:56637750..56639788hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg382039
hg192039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036306
Samples
Known GenesTEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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