A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596328



Internal ID6983645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61077232..61108567hg38UCSC Ensembl
chr3:61062905..61094240hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3831336
hg1931336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv894e214
Supporting Variantsessv11025981
SamplesHG01256
Known GenesFHIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596328
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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