A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601279



Internal ID6988317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87522419..87588669hg38UCSC Ensembl
chr4:88443571..88509821hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3866251
hg1966251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11527643
SamplesHG03240
Known GenesSPARCL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601279
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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