A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657701



Internal ID9577120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36181440..36225278hg38UCSC Ensembl
Outerchr17:36181069..36225648hg38UCSC Ensembl
Innerchr17:34508816..34552722hg19UCSC Ensembl
Outerchr17:34508445..34553092hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3844580
hg1944648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv545e199
Supporting Variantsessv6074472, essv5930654, essv5867370, essv6428347
SamplesHG01521, HG01522, HG01515, HG01516
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657701
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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