A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891800



Internal ID18839510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46197060..46269108hg38UCSC Ensembl
Outerchr10:46166132..46281263hg38UCSC Ensembl
Innerchr10:47568296..47640344hg19UCSC Ensembl
Outerchr10:47537368..47652499hg19UCSC Ensembl
Innerchr10:47038302..47110350hg18UCSC Ensembl
Outerchr10:47007374..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38115132
hg19115132
hg18115132
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791255, essv25787428, essv25788010, essv25779528, essv25783943, essv25791416, essv25790697, essv25783839, essv25791094, essv25796884, essv25783240, essv25797312, essv25786440, essv25782567, essv25801655, essv25782773
Samples
Known GenesANTXRLP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891800
Frequency
Sample Size3017
Observed Gain5
Observed Loss11
Observed Complex0
Frequencyn/a


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