A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15601063



Internal ID4400391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5869326..5888585hg38UCSC Ensembl
chr17:5772646..5791905hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3819260
hg1919260
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639824
Supporting Variants
SamplesHG03919
Known GenesLOC339166
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15601063
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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