A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896244



Internal ID22671333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210923925..210924432hg38UCSC Ensembl
chr2:211788649..211789156hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896244
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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