A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625922



Internal ID6666070
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090151
SamplesNA19207
Known GenesCD44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625922
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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