A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610079



Internal ID6996998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96747009..96762945hg38UCSC Ensembl
Innerchr6:96747509..96762445hg38UCSC Ensembl
Outerchr6:96746009..96763945hg38UCSC Ensembl
chr6:97194885..97210821hg19UCSC Ensembl
Innerchr6:97195385..97210321hg19UCSC Ensembl
Outerchr6:97193885..97211821hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3815937
hg1915937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12473062, essv12473061, essv12473063
SamplesNA11830, HG00182, NA20810
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610079
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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