A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595035



Internal ID6635310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2574118..2575408hg38UCSC Ensembl
Innerchr3:2574129..2575398hg38UCSC Ensembl
Outerchr3:2574108..2575419hg38UCSC Ensembl
chr3:2615802..2617092hg19UCSC Ensembl
Innerchr3:2615813..2617082hg19UCSC Ensembl
Outerchr3:2615792..2617103hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381291
hg191291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10899617, essv10899619, essv10899622, essv10899618, essv10899620, essv10899621
SamplesNA19030, NA19819, NA19451, HG02805, NA19471, NA19429
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595035
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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