A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434768



Internal ID14935036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43913487..43913506hg38UCSC Ensembl
Innerchr11:43913483..43913510hg38UCSC Ensembl
Outerchr11:43913464..43913529hg38UCSC Ensembl
chr11:43935037..43935056hg19UCSC Ensembl
Innerchr11:43935033..43935060hg19UCSC Ensembl
Outerchr11:43935014..43935079hg19UCSC Ensembl
chr11:43891613..43891632hg18UCSC Ensembl
Innerchr11:43891636..43891609hg18UCSC Ensembl
Outerchr11:43891590..43891655hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9652392
SamplesNA12814
Known GenesALKBH3, ALKBH3-AS1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434768
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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