A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797971



Internal ID19179195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70364351..70386524hg38UCSC Ensembl
Innerchr4:71230068..71252241hg19UCSC Ensembl
Innerchr4:71264657..71286830hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3822174
hg1922174
hg1822174
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893960
Supporting Variants
Samples
Known GenesSMR3A, SMR3B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797971
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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