A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881519



Internal ID22656495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178922965..178927748hg38UCSC Ensembl
chr1:178892100..178896883hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg384784
hg194784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881519
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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