A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5513296



Internal ID9647333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154401285..154433299hg38UCSC Ensembl
chr2:155257797..155289811hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3832015
hg1932015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658246
Supporting Variants
SamplesNA19379
Known GenesGALNT13
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5513296
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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