A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607923



Internal ID6994854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3159241..3179129hg38UCSC Ensembl
Innerchr6:3159391..3178979hg38UCSC Ensembl
Outerchr6:3159091..3179279hg38UCSC Ensembl
chr6:3159475..3179363hg19UCSC Ensembl
Innerchr6:3159625..3179213hg19UCSC Ensembl
Outerchr6:3159325..3179513hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3819889
hg1919889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1162e214
Supporting Variantsessv12178838, essv12178840, essv12178839
SamplesNA19917, NA19143, NA19248
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607923
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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