A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792901



Internal ID19163944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143905582..144009464hg38UCSC Ensembl
Innerchr1:120801479..120905064hg19UCSC Ensembl
Innerchr1:120603002..120706587hg18UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38103883
hg19103586
hg18103586
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894067
Supporting Variants
Samples
Known GenesFAM72B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792901
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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