A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625933



Internal ID6666081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35442882..35444651hg38UCSC Ensembl
Innerchr11:35442891..35444643hg38UCSC Ensembl
Outerchr11:35442874..35444660hg38UCSC Ensembl
chr11:35464430..35466199hg19UCSC Ensembl
Innerchr11:35464439..35466191hg19UCSC Ensembl
Outerchr11:35464422..35466208hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381770
hg191770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090414
SamplesHG03714
Known GenesPAMR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625933
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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