A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6538630



Internal ID9282768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36081017..36109417hg38UCSC Ensembl
chr17:34408375..34436810hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3828401
hg1928436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670934
Supporting Variants
SamplesNA12751
Known GenesCCL3, CCL4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6538630
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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