A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639659



Internal ID7026437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:939223..948350hg38UCSC Ensembl
chr17:842463..851590hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg389128
hg199128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15578159, essv15578158
SamplesHG00130, HG01628
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639659
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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