A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874471



Internal ID22649423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236113456..236204169hg38UCSC Ensembl
chr1:236276756..236367469hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3890714
hg1990714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352220
Samples
Known GenesGPR137B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874471
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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