A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090154



Internal ID4091970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35198319..35214662hg38UCSC Ensembl
Innerchr11:35198319..35214662hg38UCSC Ensembl
Outerchr11:35197819..35215162hg38UCSC Ensembl
chr11:35219866..35236209hg19UCSC Ensembl
Innerchr11:35219866..35236209hg19UCSC Ensembl
Outerchr11:35219366..35236709hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3816344
hg1916344
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625924
Supporting Variants
SamplesNA19207
Known GenesCD44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090154
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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