A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598239



Internal ID6985375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153863008..153896754hg38UCSC Ensembl
chr3:153580797..153614543hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3833747
hg1933747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11190035, essv11190029, essv11190034, essv11190027, essv11190025, essv11190028, essv11190033, essv11190032, essv11190031, essv11190026, essv11190030
SamplesNA18565, HG02058, NA19089, HG00674, NA18564, HG01866, NA18591, HG02398, HG02373, HG01600, HG03815
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598239
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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