A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589907



Internal ID6977237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15144877..15147919hg38UCSC Ensembl
Innerchr2:15144881..15147915hg38UCSC Ensembl
Outerchr2:15144873..15147923hg38UCSC Ensembl
chr2:15285001..15288043hg19UCSC Ensembl
Innerchr2:15285005..15288039hg19UCSC Ensembl
Outerchr2:15284997..15288047hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg383043
hg193043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10416073, essv10416083, essv10416070, essv10416085, essv10416072, essv10416082, essv10416075, essv10416078, essv10416071, essv10416074, essv10416079, essv10416080, essv10416076, essv10416086, essv10416081, essv10416084, essv10416087, essv10416069, essv10416077
SamplesNA18881, HG03115, NA19092, HG02870, NA19098, HG01997, NA18923, NA20287, HG03583, HG02882, HG03132, NA18871, HG02256, NA20276, HG01551, HG03103, NA19093, HG03410, HG01097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589907
Frequency
Sample Size2504
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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