A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6112276



Internal ID9089679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71599925..71899918hg38UCSC Ensembl
chr11:71310971..71610964hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38299994
hg19299994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658771
Supporting Variants
SamplesNA19057
Known GenesALG1L9P, DEFB108B, FAM86C1, LOC100129216, LOC100133315, ZNF705E
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6112276
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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