A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515072



Internal ID20888429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17116937..17119243hg38UCSC Ensembl
chr17:17020251..17022557hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382307
hg192307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034082
Samples
Known GenesMPRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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