A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510167



Internal ID20883483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9384513..9418651hg38UCSC Ensembl
chr17:9287830..9321968hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3834139
hg1934139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039131
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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