A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595084



Internal ID6982403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4092194..4130816hg38UCSC Ensembl
Innerchr3:4092694..4130316hg38UCSC Ensembl
Outerchr3:4091194..4131816hg38UCSC Ensembl
chr3:4133878..4172500hg19UCSC Ensembl
Innerchr3:4134378..4172000hg19UCSC Ensembl
Outerchr3:4132878..4173500hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3838623
hg1938623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv865e214
Supporting Variantsessv10903607, essv10903605, essv10903601, essv10903602, essv10903617, essv10903608, essv10903614, essv10903604, essv10903615, essv10903599, essv10903606, essv10903600, essv10903598, essv10903616, essv10903611, essv10903610, essv10903613, essv10903609, essv10903612, essv10903603
SamplesHG00766, NA18877, HG02600, HG03518, NA19098, HG03199, HG01046, NA19385, HG03814, HG02427, NA19327, NA20903, HG04054, HG02256, NA20542, NA19019, HG03433, HG00728, NA20502, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595084
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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