A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635806



Internal ID7022604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22786232..23120073hg38UCSC Ensembl
chr15:22752995..23086836hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38333842
hg19333842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15174352, essv15174351
SamplesHG00236, HG02075
Known GenesCYFIP1, NIPA1, NIPA2, TUBGCP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635806
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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