A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595083



Internal ID6982402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4084346..4217948hg38UCSC Ensembl
chr3:4126030..4259632hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38133603
hg19133603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv864e214
Supporting Variantsessv10903592, essv10903588, essv10903579, essv10903596, essv10903591, essv10903586, essv10903595, essv10903580, essv10903587, essv10903593, essv10903576, essv10903594, essv10903590, essv10903583, essv10903589, essv10903575, essv10903585, essv10903574, essv10903584, essv10903581, essv10903578, essv10903577, essv10903582, essv10903597
SamplesHG01985, HG00766, NA18877, HG02600, HG03518, NA19098, HG03199, HG03986, HG01046, NA19385, HG03814, HG02427, NA18557, NA19327, HG02221, NA20903, HG02256, NA20542, HG03934, NA19019, HG03433, NA19779, HG00728, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595083
Frequency
Sample Size2504
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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