A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944474



Internal ID21364543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157862573..157862884hg38UCSC Ensembl
chr2:158719085..158719396hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177767
SamplesHG002
Known GenesACVR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944474
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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