A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789343



Internal ID19160559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26559277..26600894hg38UCSC Ensembl
Innerchr10:26848206..26889823hg19UCSC Ensembl
Innerchr10:26888212..26929829hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3841618
hg1941618
hg1841618
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891778
Supporting Variants
Samples
Known GenesAPBB1IP, LINC00264
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789343
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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