A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779427



Internal ID18833310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3460878..3512044hg38UCSC Ensembl
Innerchr1:3377442..3428608hg19UCSC Ensembl
Innerchr1:3367302..3418468hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3851167
hg1951167
hg1851167
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893545
Supporting Variants
Samples
Known GenesARHGEF16, MEGF6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779427
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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