A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911486



Internal ID22686700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36926139..36926365hg38UCSC Ensembl
chr7:36965744..36965970hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449086
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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