A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587549



Internal ID6974972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152435939..152464374hg38UCSC Ensembl
chr1:152408415..152436850hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3828436
hg1928436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10145934, essv10145932, essv10145933, essv10145935
SamplesHG00608, HG01849, HG00656, HG02186
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587549
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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