A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5629324



Internal ID8606727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36182836..36224278hg38UCSC Ensembl
Outerchr17:36182365..36224848hg38UCSC Ensembl
Innerchr17:34510216..34551722hg19UCSC Ensembl
Outerchr17:34509745..34552292hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3842484
hg1942548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676887
Supporting Variants
SamplesHG01183
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5629324
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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