A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507094



Internal ID20880382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28368573..28369057hg38UCSC Ensembl
chr17:26695594..26696078hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191805
Samples
Known GenesVTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507094
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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