A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600555



Internal ID6640817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55561652..55635750hg38UCSC Ensembl
chr4:56427819..56501917hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3874099
hg1974099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11440104
SamplesNA20759
Known GenesNMU, PDCL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600555
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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