A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444122



Internal ID21101675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97295038..97295706hg38UCSC Ensembl
chr9:100057320..100057988hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194767
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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