A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7566284



Internal ID10844566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39374481..39530481hg38UCSC Ensembl
Innerchr8:39232000..39388000hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38156001
hg19156001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3296717
Supporting Variants
SamplesHuRef
Known GenesADAM3A, ADAM5
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7566284
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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