A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599863



Internal ID6986908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21302074..21317819hg38UCSC Ensembl
chr4:21303697..21319442hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3815746
hg1915746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv992e214
Supporting Variantsessv11367479
SamplesHG02339
Known GenesKCNIP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599863
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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