A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616942



Internal ID7003828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39242615..39265693hg38UCSC Ensembl
chr8:39100134..39123212hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3823079
hg1923079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13170743
SamplesHG00356
Known GenesADAM32
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616942
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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