A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875677



Internal ID22650635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187072838..187075611hg38UCSC Ensembl
chr1:187041970..187044743hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg382774
hg192774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875677
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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