A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893426



Internal ID19184246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:136353829..136566416hg38UCSC Ensembl
Outerchr2:136353829..136566416hg38UCSC Ensembl
Innerchr2:137111399..137323986hg19UCSC Ensembl
Outerchr2:137111399..137323986hg19UCSC Ensembl
Innerchr2:136827869..137040456hg18UCSC Ensembl
Outerchr2:136827869..137040456hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38212588
hg19212588
hg18212588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799384
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893426
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer