A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636041



Internal ID7022837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30962518..30964114hg38UCSC Ensembl
Innerchr15:30962518..30964114hg38UCSC Ensembl
Outerchr15:30962239..30964436hg38UCSC Ensembl
chr15:31254721..31256317hg19UCSC Ensembl
Innerchr15:31254721..31256317hg19UCSC Ensembl
Outerchr15:31254442..31256639hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381597
hg191597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15204051, essv15204048, essv15204049, essv15204046, essv15204050, essv15204047
SamplesHG01986, HG01779, HG02854, HG00369, HG03479, HG01372
Known GenesMTMR10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636041
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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