A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797091



Internal ID19167183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:61540727..61552940hg38UCSC Ensembl
Innerchr4:62406445..62418658hg19UCSC Ensembl
Innerchr4:62089040..62101253hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3812214
hg1912214
hg1812214
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893929
Supporting Variants
Samples
Known GenesLPHN3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797091
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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