A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15682126



Internal ID5683942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45638694..45657745hg38UCSC Ensembl
chr17:43716060..43735111hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3819052
hg1919052
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640670
Supporting Variants
SamplesHG02778
Known GenesCRHR1, CRHR1-IT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15682126
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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