A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778340



Internal ID18813896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30626045..30672369hg38UCSC Ensembl
Innerchr15:30918248..30964572hg19UCSC Ensembl
Innerchr15:28705540..28751864hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3846325
hg1946325
hg1846325
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892646
Supporting Variants
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778340
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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