A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907150



Internal ID22682355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49606137..49606196hg38UCSC Ensembl
chr3:49643570..49643629hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428126
Samples
Known GenesBSN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907150
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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