A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596935



Internal ID6984249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88656786..88666487hg38UCSC Ensembl
Innerchr3:88656786..88666487hg38UCSC Ensembl
Outerchr3:88656286..88666987hg38UCSC Ensembl
chr3:88705936..88715637hg19UCSC Ensembl
Innerchr3:88705936..88715637hg19UCSC Ensembl
Outerchr3:88705436..88716137hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg389702
hg199702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11068002, essv11068016, essv11067996, essv11068017, essv11068005, essv11068000, essv11068008, essv11068006, essv11068009, essv11068015, essv11068011, essv11067999, essv11068007, essv11068001, essv11068014, essv11068003, essv11068012, essv11067997, essv11067994, essv11068018, essv11067995, essv11068013, essv11067998, essv11068010, essv11068004
SamplesHG01060, HG01918, HG01944, HG01947, HG02146, HG02266, HG01354, HG01893, HG01967, HG02265, HG01360, HG02102, NA19740, HG01842, HG01572, HG02127, HG01992, HG00734, HG01939, HG02274, NA19783, NA19785, HG02348, HG01920, HG02425
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596935
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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