A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443375



Internal ID21100928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113351203..113351631hg38UCSC Ensembl
chr9:116113483..116113911hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174388
Samples
Known GenesBSPRY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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