A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595942



Internal ID6983260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39956794..39974643hg38UCSC Ensembl
Innerchr3:39957294..39974143hg38UCSC Ensembl
Outerchr3:39955794..39975643hg38UCSC Ensembl
chr3:39998285..40016134hg19UCSC Ensembl
Innerchr3:39998785..40015634hg19UCSC Ensembl
Outerchr3:39997285..40017134hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3817850
hg1917850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv886e214
Supporting Variantsessv10987979, essv10987980
SamplesHG00699, HG02406
Known GenesMYRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595942
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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