A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596585



Internal ID6983899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74913126..74922101hg38UCSC Ensembl
chr3:74962277..74971252hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg388976
hg198976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv901e214
Supporting Variantsessv11040430
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596585
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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