A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13770725



Internal ID3750039
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623102
Supporting Variants
SamplesHG03380
Known GenesZFAND4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13770725
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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