A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668396



Internal ID9587815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71592769..71892787hg38UCSC Ensembl
chr11:71303815..71603833hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38300019
hg19300019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv223e199
Supporting Variantsessv6194834
SamplesNA19390
Known GenesALG1L9P, DEFB108B, FAM86C1, LOC100129216, LOC100133315, ZNF705E
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668396
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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