A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13586773



Internal ID1594056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102616863..102768576hg38UCSC Ensembl
chr9:105379145..105530858hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38151714
hg19151714
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621284
Supporting Variants
SamplesHG01485
Known GenesLINC00587
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13586773
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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