A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909466



Internal ID22684676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18412351..18425692hg38UCSC Ensembl
chr7:18451974..18465315hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813342
hg1913342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439690
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909466
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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