A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791400



Internal ID18824255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:130128318..130391244hg38UCSC Ensembl
Innerchr2:130885891..131148817hg19UCSC Ensembl
Innerchr2:130602361..130865287hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38262927
hg19262927
hg18262927
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=42
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791400
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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