A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620690



Internal ID7007560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74090713..74091391hg38UCSC Ensembl
Innerchr9:74090714..74091390hg38UCSC Ensembl
Outerchr9:74090712..74091392hg38UCSC Ensembl
chr9:76705629..76706307hg19UCSC Ensembl
Innerchr9:76705630..76706306hg19UCSC Ensembl
Outerchr9:76705628..76706308hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13520062, essv13520077, essv13520076, essv13520069, essv13520068, essv13520060, essv13520074, essv13520059, essv13520063, essv13520067, essv13520065, essv13520075, essv13520070, essv13520064, essv13520071, essv13520061, essv13520073, essv13520072, essv13520066
SamplesHG03517, HG02798, HG02804, HG03385, HG02952, NA19138, HG02479, NA19347, NA19152, HG02144, HG02887, HG02429, HG02979, HG01890, HG02807, HG02501, HG01551, HG02274, NA19430
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620690
Frequency
Sample Size2504
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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