A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13704055



Internal ID6134781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14969228..15018085hg38UCSC Ensembl
chr10:15011227..15060084hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3848858
hg1948858
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622434
Supporting Variants
SamplesNA19669
Known GenesMEIG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13704055
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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