A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436268



Internal ID21093821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109041548..109042846hg38UCSC Ensembl
chr9:111803828..111805126hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381299
hg191299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173137
Samples
Known GenesTMEM245
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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