A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786819



Internal ID19167806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:113671..143973hg38UCSC Ensembl
Innerchr18:113671..143973hg19UCSC Ensembl
Innerchr18:103671..133973hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3830303
hg1930303
hg1830303
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893054
Supporting Variants
Samples
Known GenesROCK1P1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786819
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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