A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13732564



Internal ID3734380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27071518..27136388hg38UCSC Ensembl
chr10:27360447..27425317hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3864871
hg1964871
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622707
Supporting Variants
SamplesHG04164
Known GenesANKRD26, YME1L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13732564
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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