A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5507485



Internal ID8484888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59550320..59641606hg38UCSC Ensembl
Outerchr15:59550283..59641656hg38UCSC Ensembl
Innerchr15:59842519..59933805hg19UCSC Ensembl
Outerchr15:59842482..59933855hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3891374
hg1991374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668729
Supporting Variants
SamplesNA20790
Known GenesGCNT3, GTF2A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5507485
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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