A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502125



Internal ID20875367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9468217..9478330hg38UCSC Ensembl
chr17:9371534..9381647hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3810114
hg1910114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181145
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502125
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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