A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497440



Internal ID20870646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31963369..31963787hg38UCSC Ensembl
chr17:30290388..30290806hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034925
Samples
Known GenesSUZ12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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