A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918012



Internal ID22693233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74126912..74126963hg38UCSC Ensembl
chr9:76741828..76741879hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437969
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918012
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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