A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880069



Internal ID22655039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38669004..38715801hg38UCSC Ensembl
chr1:39134676..39181473hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3846798
hg1946798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880069
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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