A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090151



Internal ID4091967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35148319..35190916hg38UCSC Ensembl
Innerchr11:35148319..35190916hg38UCSC Ensembl
Outerchr11:35147819..35191416hg38UCSC Ensembl
chr11:35169866..35212463hg19UCSC Ensembl
Innerchr11:35169866..35212463hg19UCSC Ensembl
Outerchr11:35169366..35212963hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3842598
hg1942598
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625922
Supporting Variants
SamplesNA19207
Known GenesCD44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090151
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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