A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498817



Internal ID20872030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28692261..28692938hg38UCSC Ensembl
chr17:27019279..27019956hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035195
Samples
Known GenesSUPT6H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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