A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876674



Internal ID22651635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37241008..37245775hg38UCSC Ensembl
chr1:37706609..37711376hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg384768
hg194768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876674
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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