A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870657



Internal ID22645593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25960365..25960490hg38UCSC Ensembl
chr2:26183234..26183359hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407333
Samples
Known GenesKIF3C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870657
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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