A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3975n223



Internal ID22806943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88756701..88871000hg38UCSC Ensembl
chr2:89056218..89170516hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38114300
hg19114299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6345672, nsv6346748
Samples
Known GenesANKRD36BP2, MIR4436A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3975n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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