A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783921



Internal ID18829205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16913478..16955930hg38UCSC Ensembl
Innerchr1:17239973..17282425hg19UCSC Ensembl
Innerchr1:17112560..17155012hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842453
hg1942453
hg1842453
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892525
Supporting Variants
Samples
Known GenesCROCC
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783921
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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