A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8653063



Internal ID15106987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94640025..94640025hg38UCSC Ensembl
Innerchr11:94640024..94640026hg38UCSC Ensembl
Outerchr11:94639975..94640075hg38UCSC Ensembl
chr11:94373191..94373191hg19UCSC Ensembl
Innerchr11:94373190..94373192hg19UCSC Ensembl
Outerchr11:94373141..94373241hg19UCSC Ensembl
chr11:94012839..94012839hg18UCSC Ensembl
Innerchr11:94012840..94012838hg18UCSC Ensembl
Outerchr11:94012789..94012889hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38128
hg19128
hg18128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3364588
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8653063
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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