A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451517



Internal ID21109070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97276231..97282381hg38UCSC Ensembl
chr9:100038513..100044663hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386151
hg196151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184557
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451517
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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