A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878659



Internal ID22653625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219226152..219230024hg38UCSC Ensembl
chr1:219399494..219403366hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383873
hg193873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878659
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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