A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622433



Internal ID7009292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14969228..15018085hg38UCSC Ensembl
chr10:15011227..15060084hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3848858
hg1948858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704045, essv13704044, essv13704042, essv13704043
SamplesHG04096, HG03667, HG01500, HG02774
Known GenesMEIG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622433
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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