A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665441



Internal ID9931546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95504342..95504586hg38UCSC Ensembl
Outerchr5:95504185..95504739hg38UCSC Ensembl
Innerchr5:94840046..94840290hg19UCSC Ensembl
Outerchr5:94839889..94840443hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5415290, essv6083064, essv5700892, essv6417263, essv6350614, essv6002564, essv5821823, essv5713129, essv6199039, essv5779927, essv6044300, essv6169455, essv6473316, essv5650023, essv6214282, essv5851558, essv5468358, essv5822133, essv6193113
SamplesNA18508, NA18980, NA19190, NA18519, NA18942, NA18916, NA19138, NA18498, NA19239, NA19210, NA19455, NA18523, NA19834, NA18952, NA18517, NA19240, NA19129, NA19463, NA18965
Known GenesTTC37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665441
Frequency
Sample Size1151
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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