A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893016



Internal ID18837150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:44723046..44776840hg38UCSC Ensembl
Outerchr17:44723046..44776840hg38UCSC Ensembl
Innerchr17:42800414..42854208hg19UCSC Ensembl
Outerchr17:42800414..42854208hg19UCSC Ensembl
Innerchr17:40155940..40209734hg18UCSC Ensembl
Outerchr17:40155940..40209734hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3853795
hg1953795
hg1853795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799234
Samples
Known GenesADAM11, DBF4B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893016
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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