A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586184



Internal ID6626497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59531140..59570862hg38UCSC Ensembl
Innerchr1:59531140..59570862hg38UCSC Ensembl
Outerchr1:59530640..59571362hg38UCSC Ensembl
chr1:59996812..60036534hg19UCSC Ensembl
Innerchr1:59996812..60036534hg19UCSC Ensembl
Outerchr1:59996312..60037034hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3839723
hg1939723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9943925, essv9943926
SamplesHG03681, HG01779
Known GenesFGGY
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586184
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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