A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191885



Internal ID1681450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155692264..155737863hg38UCSC Ensembl
chr3:155410053..155455652hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3845600
hg1945600
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598281
Supporting Variants
SamplesHG01551
Known GenesPLCH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191885
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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