A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13633350



Internal ID6853577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131800850..131870335hg38UCSC Ensembl
chr9:134676237..134745722hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3869486
hg1969486
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621902
Supporting Variants
SamplesNA21088
Known GenesMED27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13633350
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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