A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670934



Internal ID9590353
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6437415, essv6169229, essv5841977, essv5524390, essv5929130, essv5413485, essv6324403, essv5701619, essv5836396, essv6423332, essv6538630, essv6285967, essv5444840, essv6231608, essv6434203, essv6005266, essv6345212, essv5769730, essv6148431, essv5469687, essv6372989, essv6591452, essv6536948
SamplesNA18870, NA18861, NA18871, NA18523, NA19114, NA18608, NA18542, NA18489, NA19257, NA12044, NA19147, NA19239, NA18566, NA18956, NA12751, NA19102, NA19238, NA18510, NA18558, NA18858, NA18499, NA19240, NA18853
Known GenesCCL3, CCL4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670934
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer