A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870207



Internal ID22645142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171812412..171819854hg38UCSC Ensembl
chr1:171781552..171788994hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg387443
hg197443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870207
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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