A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11735935



Internal ID1737751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185372047..185422056hg38UCSC Ensembl
chr4:186293201..186343210hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3850010
hg1950010
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603493
Supporting Variants
SamplesHG02232
Known GenesANKRD37, LRP2BP, UFSP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11735935
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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