A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11662629



Internal ID1584631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160027453..160035367hg38UCSC Ensembl
chr4:160948605..160956519hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387915
hg197915
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602855
Supporting Variants
SamplesHG01465
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11662629
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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