A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587723



Internal ID6975146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161016634..161029399hg38UCSC Ensembl
chr1:160986424..160999189hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3812766
hg1912766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10168284, essv10168282, essv10168281, essv10168283
SamplesHG02026, HG03917, HG02019, HG02032
Known GenesF11R
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587723
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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