A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10145539



Internal ID147355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151451171..151453543hg38UCSC Ensembl
Innerchr1:151451172..151453543hg38UCSC Ensembl
Outerchr1:151451171..151453544hg38UCSC Ensembl
chr1:151423647..151426019hg19UCSC Ensembl
Innerchr1:151423648..151426019hg19UCSC Ensembl
Outerchr1:151423647..151426020hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587528
Supporting Variants
SamplesHG02278
Known GenesPOGZ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10145539
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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