A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13520046



Internal ID3521862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73909488..73917605hg38UCSC Ensembl
Innerchr9:73909488..73917605hg38UCSC Ensembl
Outerchr9:73908988..73918105hg38UCSC Ensembl
chr9:76524404..76532521hg19UCSC Ensembl
Innerchr9:76524404..76532521hg19UCSC Ensembl
Outerchr9:76523904..76533021hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388118
hg198118
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620683
Supporting Variants
SamplesNA19309
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13520046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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