A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6210612



Internal ID9857661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39374547..39529503hg38UCSC Ensembl
Outerchr8:39374076..39529923hg38UCSC Ensembl
Innerchr8:39232066..39387022hg19UCSC Ensembl
Outerchr8:39231595..39387442hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155848
hg19155848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663438
Supporting Variants
SamplesNA20527
Known GenesADAM3A, ADAM5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6210612
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer