A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891802



Internal ID18839512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46370665hg38UCSC Ensembl
Outerchr10:46172086..46377652hg38UCSC Ensembl
Innerchr10:47543322..47741882hg19UCSC Ensembl
Outerchr10:47543322..47748912hg19UCSC Ensembl
Innerchr10:47013328..47211888hg18UCSC Ensembl
Outerchr10:47013328..47218918hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38205567
hg19205591
hg18205591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788367, essv25789080
Samples
Known GenesANTXRL, ANTXRLP1, ANXA8L1, ANXA8L2, FAM25B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891802
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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