A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450322



Internal ID21107875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35863826..35871371hg38UCSC Ensembl
chr9:35863823..35871368hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg387546
hg197546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189424
Samples
Known GenesLINC00950, OR13J1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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