A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507263



Internal ID20880551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28801254..28804771hg38UCSC Ensembl
chr17:27128272..27131789hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383518
hg193518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035202
Samples
Known GenesFAM222B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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