A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15635774



Internal ID5650969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17605123..17611823hg38UCSC Ensembl
Innerchr17:17605150..17611796hg38UCSC Ensembl
Outerchr17:17605096..17611850hg38UCSC Ensembl
chr17:17508437..17515137hg19UCSC Ensembl
Innerchr17:17508464..17515110hg19UCSC Ensembl
Outerchr17:17508410..17515164hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg386701
hg196701
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640130
Supporting Variants
SamplesNA19066
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15635774
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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