A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526095



Internal ID20899456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65962255..66131636hg38UCSC Ensembl
chr17:63958373..64127754hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38169382
hg19169382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037887
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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