A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439997



Internal ID21097550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97318863..97340961hg38UCSC Ensembl
chr9:100081145..100103243hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3822099
hg1922099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182275
Samples
Known GenesCCDC180, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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