A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6332149



Internal ID9717252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:81505535..81512249hg38UCSC Ensembl
Outerchr3:81505378..81512402hg38UCSC Ensembl
Innerchr3:81554686..81561400hg19UCSC Ensembl
Outerchr3:81554529..81561553hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg387025
hg197025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659520
Supporting Variants
SamplesNA19469
Known GenesGBE1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6332149
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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