A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597886



Internal ID6985024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136253462..136254638hg38UCSC Ensembl
Innerchr3:136253462..136254638hg38UCSC Ensembl
Outerchr3:136253192..136254915hg38UCSC Ensembl
chr3:135972304..135973480hg19UCSC Ensembl
Innerchr3:135972304..135973480hg19UCSC Ensembl
Outerchr3:135972034..135973757hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11156822, essv11156830, essv11156820, essv11156825, essv11156828, essv11156821, essv11156829, essv11156824, essv11156823, essv11156819, essv11156826, essv11156827
SamplesNA21097, HG00315, NA19684, HG01513, HG00130, HG00326, HG00188, NA20535, NA20504, HG00288, HG01085, HG00123
Known GenesPCCB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597886
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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