A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009338



Internal ID7073858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3358764..3358772hg38UCSC Ensembl
chr11:3379994..3380002hg19UCSC Ensembl
chr11:3336570..3336578hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3575023
SamplesHuRef
Known GenesZNF195
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009338
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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