A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449650



Internal ID21107203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97934488..97936361hg38UCSC Ensembl
chr9:100696770..100698643hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381874
hg191874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184705
Samples
Known GenesHEMGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449650
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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