A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13541798



Internal ID3543614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83892470..83902574hg38UCSC Ensembl
chr9:86507385..86517489hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3810105
hg1910105
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620908
Supporting Variants
SamplesHG03268
Known GenesKIF27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13541798
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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