A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761082



Internal ID22095578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97410945..97411057hg38UCSC Ensembl
chr9:100173227..100173339hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761082
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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