A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026699



Internal ID21936042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7599981..7600043hg38UCSC Ensembl
chr17:7503299..7503361hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618497
Samples
Known GenesFXR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026699
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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