A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799238



Internal ID19180614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:135218928..135372221hg38UCSC Ensembl
Innerchr2:135976498..136129791hg19UCSC Ensembl
Innerchr2:135692968..135846261hg18UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38153294
hg19153294
hg18153294
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893415
Supporting Variants
Samples
Known GenesZRANB3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799238
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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