A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620683



Internal ID6660864
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13520046
SamplesNA19309
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620683
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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