A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663321



Internal ID9929426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168074244..168074866hg38UCSC Ensembl
Outerchr6:168074207..168074916hg38UCSC Ensembl
Innerchr6:168474924..168475546hg19UCSC Ensembl
Outerchr6:168474887..168475596hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5903155, essv5578419, essv5501641
SamplesNA19075, NA18557, NA19074
Known GenesFRMD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663321
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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