A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868984



Internal ID22643919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24668147..24670672hg38UCSC Ensembl
chr1:24994638..24997163hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382526
hg192526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352477
Samples
Known GenesSRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868984
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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