A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901255



Internal ID22676404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234575413..234580143hg38UCSC Ensembl
chr2:235484057..235488787hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg384731
hg194731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901255
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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