A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892943



Internal ID19183763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:900770..917084hg38UCSC Ensembl
Outerchr17:900770..917084hg38UCSC Ensembl
Innerchr17:804010..820324hg19UCSC Ensembl
Outerchr17:804010..820324hg19UCSC Ensembl
Innerchr17:750760..767074hg18UCSC Ensembl
Outerchr17:750760..767074hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3816315
hg1916315
hg1816315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800165, essv25782615, essv25800201, essv25784243, essv25785733
Samples
Known GenesNXN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892943
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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