A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15630732



Internal ID4071589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16670157..16686323hg38UCSC Ensembl
Innerchr17:16670657..16685823hg38UCSC Ensembl
Outerchr17:16669157..16687323hg38UCSC Ensembl
chr17:16573471..16589637hg19UCSC Ensembl
Innerchr17:16573971..16589137hg19UCSC Ensembl
Outerchr17:16572471..16590637hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3816167
hg1916167
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640112
Supporting Variants
SamplesHG03705
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15630732
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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