A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511565



Internal ID20884894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38639741..38645728hg38UCSC Ensembl
chr17:36795994..36801981hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385988
hg195988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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