A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598176



Internal ID6985312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151489728..151501073hg38UCSC Ensembl
Innerchr3:151489728..151501073hg38UCSC Ensembl
Outerchr3:151489228..151501573hg38UCSC Ensembl
chr3:151207516..151218861hg19UCSC Ensembl
Innerchr3:151207516..151218861hg19UCSC Ensembl
Outerchr3:151207016..151219361hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3811346
hg1911346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11185918, essv11185919, essv11185920, essv11185921
SamplesHG03589, HG03978, HG03784, HG03861
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598176
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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