A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620546



Internal ID6660728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68675237..68722866hg38UCSC Ensembl
chr9:71290153..71337782hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3847630
hg1947630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13505061
SamplesNA18943
Known GenesPIP5K1B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620546
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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