A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5903155



Internal ID9543782
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 StatusS
Merged Variantsesv2663321
Supporting Variants
SamplesNA19075
Known GenesFRMD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5903155
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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