A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897638



Internal ID22672743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44340617..44345350hg38UCSC Ensembl
chr3:44382109..44386842hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425047
Samples
Known GenesTCAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897638
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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