A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797750



Internal ID19159587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103201980..103241080hg38UCSC Ensembl
Innerchr14:103668317..103707417hg19UCSC Ensembl
Innerchr14:102738070..102777170hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3839101
hg1939101
hg1839101
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892580
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797750
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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