A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636025



Internal ID7022821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30628576..30700028hg38UCSC Ensembl
chr15:30920779..30992231hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3871453
hg1971453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15203627, essv15203641, essv15203643, essv15203640, essv15203639, essv15203626, essv15203644, essv15203623, essv15203624, essv15203642, essv15203628, essv15203637, essv15203636, essv15203631, essv15203630, essv15203638, essv15203634, essv15203635, essv15203646, essv15203632, essv15203647, essv15203629, essv15203633, essv15203645, essv15203625
SamplesHG04210, NA11830, NA18999, NA18528, HG00244, HG01802, NA19057, NA12813, NA18960, NA19054, NA18964, HG03595, HG02260, NA18985, HG01709, NA18973, NA18747, NA19077, NA18981, HG01512, HG03790, HG01894, NA18972, HG01377, HG00759
Known GenesARHGAP11B, LOC100288637
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636025
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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