A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779899



Internal ID19169485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4051127..4068463hg38UCSC Ensembl
Innerchr1:4111187..4128523hg19UCSC Ensembl
Innerchr1:4011047..4028383hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3817337
hg1917337
hg1817337
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893656
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779899
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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