A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892952



Internal ID19183772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3709996..3715237hg38UCSC Ensembl
Outerchr17:3709996..3715237hg38UCSC Ensembl
Innerchr17:3613290..3618531hg19UCSC Ensembl
Outerchr17:3613290..3618531hg19UCSC Ensembl
Innerchr17:3560039..3565280hg18UCSC Ensembl
Outerchr17:3560039..3565280hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg385242
hg195242
hg185242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800444, essv25778859
Samples
Known GenesITGAE
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892952
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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