A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804891



Internal ID21250229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100037414..100037557hg38UCSC Ensembl
chr2:100653876..100654019hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689632
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804891
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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