A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636467



Internal ID7023261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51528006..51528780hg38UCSC Ensembl
Innerchr15:51528030..51528757hg38UCSC Ensembl
Outerchr15:51527983..51528804hg38UCSC Ensembl
chr15:51820203..51820977hg19UCSC Ensembl
Innerchr15:51820227..51820954hg19UCSC Ensembl
Outerchr15:51820180..51821001hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15248584, essv15248583, essv15248582, essv15248581, essv15248585
SamplesHG02337, HG02485, NA19725, HG00149, HG00254
Known GenesDMXL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636467
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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