A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6308026



Internal ID9285429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82628241..82789040hg38UCSC Ensembl
Innerchr15:83296992..83457792hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38160800
hg19160801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674021
Supporting Variants
SamplesNA12891
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6308026
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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