A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6577265



Internal ID9554668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:864834..1489637hg38UCSC Ensembl
chr11:864834..1510867hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38624804
hg19646034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669189
Supporting Variants
SamplesNA19066
Known GenesAP2A2, BRSK2, CHID1, MIR6744, MOB2, MUC2, MUC5B, MUC6, TOLLIP, TOLLIP-AS1, TSPAN4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6577265
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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