A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891801



Internal ID18839511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46239982..46311575hg38UCSC Ensembl
Outerchr10:46166132..46370665hg38UCSC Ensembl
Innerchr10:47611218..47682811hg19UCSC Ensembl
Outerchr10:47537368..47741882hg19UCSC Ensembl
Innerchr10:47081224..47152817hg18UCSC Ensembl
Outerchr10:47007374..47211888hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38204534
hg19204515
hg18204515
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789382, essv25788489, essv25796822, essv25789513, essv25788097, essv25787766, essv25781556, essv25789020, essv25798574, essv25788828, essv25798736, essv25788756, essv25792540, essv25781611, essv25801067, essv25792688, essv25792249, essv25782234, essv25788213, essv25787976, essv25787786, essv25798027, essv25789122, essv25779970
Samples
Known GenesANTXRL, ANTXRLP1, FAM25B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891801
Frequency
Sample Size3017
Observed Gain15
Observed Loss9
Observed Complex0
Frequencyn/a


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