A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676663



Internal ID9942768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71626150..71899506hg38UCSC Ensembl
chr11:71337196..71610552hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38273357
hg19273357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv223e199
Supporting Variantsessv6356807
SamplesNA12718
Known GenesALG1L9P, DEFB108B, FAM86C1, LOC100129216, LOC100133315, ZNF705E
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676663
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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