A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625907



Internal ID6666055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34122334..34125457hg38UCSC Ensembl
Innerchr11:34122334..34125457hg38UCSC Ensembl
Outerchr11:34122094..34125675hg38UCSC Ensembl
chr11:34143881..34147004hg19UCSC Ensembl
Innerchr11:34143881..34147004hg19UCSC Ensembl
Outerchr11:34143641..34147222hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383124
hg193124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14088612
SamplesHG01798
Known GenesNAT10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625907
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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