A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616956



Internal ID6657152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39657841..39689844hg38UCSC Ensembl
Innerchr8:39657841..39689844hg38UCSC Ensembl
Outerchr8:39657341..39690344hg38UCSC Ensembl
chr8:39515360..39547363hg19UCSC Ensembl
Innerchr8:39515360..39547363hg19UCSC Ensembl
Outerchr8:39514860..39547863hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3832004
hg1932004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13176361
SamplesHG02497
Known GenesADAM18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616956
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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