A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509506



Internal ID20882816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9288463..9289667hg38UCSC Ensembl
chr17:9191780..9192984hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039120
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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