A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790206



Internal ID18815202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:130080351..130390535hg38UCSC Ensembl
Innerchr2:130837924..131148108hg19UCSC Ensembl
Innerchr2:130554394..130864578hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38310185
hg19310185
hg18310185
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893326
Supporting Variants
Samples
Known GenesCCDC115, CCDC74B, IMP4, MED15P9, MZT2B, POTEF, PTPN18, SMPD4, TUBA3E
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=44
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790206
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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