A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898214



Internal ID22673327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175142701..175142825hg38UCSC Ensembl
chr2:176007429..176007553hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400101
Samples
Known GenesATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898214
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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