A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598302



Internal ID6985438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156424404..156424956hg38UCSC Ensembl
Innerchr3:156424405..156424955hg38UCSC Ensembl
Outerchr3:156424403..156424957hg38UCSC Ensembl
chr3:156142193..156142745hg19UCSC Ensembl
Innerchr3:156142194..156142744hg19UCSC Ensembl
Outerchr3:156142192..156142746hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11193190
SamplesHG01924
Known GenesKCNAB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598302
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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