A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13520023



Internal ID3229384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73837314..73851612hg38UCSC Ensembl
Innerchr9:73837314..73851612hg38UCSC Ensembl
Outerchr9:73836814..73852112hg38UCSC Ensembl
chr9:76452230..76466528hg19UCSC Ensembl
Innerchr9:76452230..76466528hg19UCSC Ensembl
Outerchr9:76451730..76467028hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3814299
hg1914299
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620680
Supporting Variants
SamplesHG02839
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13520023
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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