A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893085



Internal ID18837219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31387447..31429446hg38UCSC Ensembl
Outerchr18:31384800..31429446hg38UCSC Ensembl
Innerchr18:28967410..29009409hg19UCSC Ensembl
Outerchr18:28964763..29009409hg19UCSC Ensembl
Innerchr18:27221408..27263407hg18UCSC Ensembl
Outerchr18:27218761..27263407hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3844647
hg1944647
hg1844647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786352, essv25801668, essv25799763, essv25783612, essv25784266, essv25783482, essv25801641, essv25785278, essv25798925
Samples
Known GenesDSG4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893085
Frequency
Sample Size3017
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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