A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435650



Internal ID22493520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74090703..74091373hg38UCSC Ensembl
chr9:76705619..76706289hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910983
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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