A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846453



Internal ID22621388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23099952..23104676hg38UCSC Ensembl
chr7:23139571..23144295hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384725
hg194725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504770
Samples
Known GenesKLHL7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846453
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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