A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891535



Internal ID18839245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5306824..5324922hg38UCSC Ensembl
Outerchr9:5302095..5335470hg38UCSC Ensembl
Innerchr9:5306824..5324922hg19UCSC Ensembl
Outerchr9:5302095..5335470hg19UCSC Ensembl
Innerchr9:5296824..5314922hg18UCSC Ensembl
Outerchr9:5292095..5325470hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3833376
hg1933376
hg1833376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786190, essv25784009, essv25799838, essv25797475, essv25801204, essv25799173, essv25799484, essv25796743, essv25785195, essv25781499, essv25780171, essv25786035, essv25796421, essv25783245, essv25797518, essv25782348, essv25779390, essv25796610, essv25798607, essv25784293, essv25779730, essv25778884, essv25796594, essv25782376, essv25782292, essv25785357, essv25779624, essv25782697, essv25796935, essv25778273, essv25783730, essv25784094, essv25778491, essv25796398, essv25797694, essv25787019, essv25798989, essv25801240
Samples
Known GenesRLN1, RLN2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891535
Frequency
Sample Size3017
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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