A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621284



Internal ID7008153
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13586773
SamplesHG01485
Known GenesLINC00587
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621284
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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