A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11735934



Internal ID1737750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185370615..185448567hg38UCSC Ensembl
chr4:186291769..186369721hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3877953
hg1977953
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603492
Supporting Variants
SamplesHG02232
Known GenesANKRD37, C4orf47, CCDC110, LRP2BP, UFSP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11735934
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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