A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13027573



Internal ID4457088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154278700..154305535hg38UCSC Ensembl
chr7:153975785..154002620hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3826836
hg1926836
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615597
Supporting Variants
SamplesHG03965
Known GenesDPP6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13027573
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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