A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622362



Internal ID7009221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12152352..12153876hg38UCSC Ensembl
Innerchr10:12152352..12153876hg38UCSC Ensembl
Outerchr10:12152251..12153951hg38UCSC Ensembl
chr10:12194351..12195875hg19UCSC Ensembl
Innerchr10:12194351..12195875hg19UCSC Ensembl
Outerchr10:12194250..12195950hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381525
hg191525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13696267
SamplesHG01991
Known GenesSEC61A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622362
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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