A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13177138



Internal ID3391830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40015808..40052207hg38UCSC Ensembl
chr8:39873327..39909726hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3836400
hg1936400
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616964
Supporting Variants
SamplesHG03040
Known GenesIDO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13177138
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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