A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893415



Internal ID19184235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:135218928..135372221hg38UCSC Ensembl
Outerchr2:135218928..135372221hg38UCSC Ensembl
Innerchr2:135976498..136129791hg19UCSC Ensembl
Outerchr2:135976498..136129791hg19UCSC Ensembl
Innerchr2:135692968..135846261hg18UCSC Ensembl
Outerchr2:135692968..135846261hg18UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38153294
hg19153294
hg18153294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799238
Samples
Known GenesZRANB3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893415
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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