A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624093



Internal ID7010949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86561568..86566540hg38UCSC Ensembl
Innerchr10:86561589..86566520hg38UCSC Ensembl
Outerchr10:86561548..86566561hg38UCSC Ensembl
chr10:88321325..88326297hg19UCSC Ensembl
Innerchr10:88321346..88326277hg19UCSC Ensembl
Outerchr10:88321305..88326318hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg384973
hg194973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13883962, essv13883961, essv13883959, essv13883963, essv13883964, essv13883960
SamplesHG02624, HG02623, HG02666, HG02667, NA19434, NA19467
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624093
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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