A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598768



Internal ID6985903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176476932..176480156hg38UCSC Ensembl
Innerchr3:176476945..176480143hg38UCSC Ensembl
Outerchr3:176476919..176480169hg38UCSC Ensembl
chr3:176194720..176197944hg19UCSC Ensembl
Innerchr3:176194733..176197931hg19UCSC Ensembl
Outerchr3:176194707..176197957hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383225
hg193225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11236081, essv11236071, essv11236074, essv11236087, essv11236084, essv11236088, essv11236086, essv11236089, essv11236079, essv11236069, essv11236070, essv11236082, essv11236075, essv11236077, essv11236072, essv11236073, essv11236083, essv11236080, essv11236076, essv11236085, essv11236078
SamplesHG01610, HG00361, HG00242, NA19819, NA12400, HG00261, NA12155, HG01503, HG01488, HG01528, HG00369, HG00190, NA20903, HG03660, NA20856, HG00140, HG00254, HG00339, HG00125, HG02238, NA11832
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598768
Frequency
Sample Size2504
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer