A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514280



Internal ID20887632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39945569..39947900hg38UCSC Ensembl
chr17:38101822..38104153hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg382332
hg192332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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