A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500585



Internal ID20873812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35592501..35601700hg38UCSC Ensembl
chr17:33919520..33928719hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177550
Samples
Known GenesAP2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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