A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800135



Internal ID18820649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43596778..43647444hg38UCSC Ensembl
Innerchr15:43888976..43939642hg19UCSC Ensembl
Innerchr15:41676268..41726934hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3850667
hg1950667
hg1850667
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892682
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1B, RNU6-28P, STRC
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800135
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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