A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877400



Internal ID22652365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:96801602..96801655hg38UCSC Ensembl
chr2:97467339..97467392hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403951
Samples
Known GenesCNNM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877400
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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