A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636817



Internal ID7023611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69023700..69025355hg38UCSC Ensembl
Innerchr15:69023709..69025347hg38UCSC Ensembl
Outerchr15:69023692..69025364hg38UCSC Ensembl
chr15:69316040..69317695hg19UCSC Ensembl
Innerchr15:69316049..69317687hg19UCSC Ensembl
Outerchr15:69316032..69317704hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15279748, essv15279758, essv15279753, essv15279759, essv15279752, essv15279756, essv15279760, essv15279771, essv15279754, essv15279764, essv15279766, essv15279751, essv15279747, essv15279763, essv15279769, essv15279749, essv15279761, essv15279762, essv15279768, essv15279757, essv15279767, essv15279750, essv15279765, essv15279770, essv15279755
SamplesHG02870, HG02624, HG02769, HG02840, NA20317, HG02860, HG03209, HG02571, NA18520, HG02882, NA18934, HG03547, HG02450, HG02887, NA18910, HG01889, HG02666, HG01403, HG02675, HG02813, HG02464, HG02814, HG03258, HG02629, HG02760
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636817
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