A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498134



Internal ID20871342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5392909..5400713hg38UCSC Ensembl
chr17:5296229..5304033hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387805
hg197805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036667
Samples
Known GenesNUP88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498134
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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