A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15601586



Internal ID1837252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6277841..6391169hg38UCSC Ensembl
chr17:6181161..6294489hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38113329
hg19113329
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639835
Supporting Variants
SamplesHG01705
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15601586
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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