A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893032



Internal ID19183852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54758465..54771723hg38UCSC Ensembl
Outerchr17:54755970..54775562hg38UCSC Ensembl
Innerchr17:52835826..52849084hg19UCSC Ensembl
Outerchr17:52833331..52852923hg19UCSC Ensembl
Innerchr17:50190825..50204083hg18UCSC Ensembl
Outerchr17:50188330..50207922hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3819593
hg1919593
hg1819593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782917, essv25782988, essv25780587
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893032
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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