A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625923



Internal ID6666071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35156506..35162212hg38UCSC Ensembl
Innerchr11:35156514..35162204hg38UCSC Ensembl
Outerchr11:35156498..35162220hg38UCSC Ensembl
chr11:35178053..35183759hg19UCSC Ensembl
Innerchr11:35178061..35183751hg19UCSC Ensembl
Outerchr11:35178045..35183767hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385707
hg195707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090153, essv14090152
SamplesNA20339, NA19207
Known GenesCD44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625923
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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