A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623102



Internal ID7009959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45666422..45677956hg38UCSC Ensembl
chr10:46161870..46173404hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3811535
hg1911535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13770725
SamplesHG03380
Known GenesZFAND4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623102
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