A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664544



Internal ID9583963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36084282..36190566hg38UCSC Ensembl
Outerchr17:36084248..36190601hg38UCSC Ensembl
Innerchr17:34411639..34517955hg19UCSC Ensembl
Outerchr17:34411605..34517990hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38106354
hg19106386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6516610
SamplesHG00705
Known GenesCCL3, CCL4, TBC1D3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664544
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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