A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780984



Internal ID19174743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68631558..68691052hg38UCSC Ensembl
Innerchr4:69497276..69556770hg19UCSC Ensembl
Innerchr4:69179871..69239365hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3859495
hg1959495
hg1859495
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893947
Supporting Variants
Samples
Known GenesUGT2B15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780984
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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