A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526673



Internal ID20900034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48951542..48989062hg38UCSC Ensembl
chr17:47028904..47066424hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3837521
hg1937521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177453
Samples
Known GenesGIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526673
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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