A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607882



Internal ID6994813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1135847..1213759hg38UCSC Ensembl
chr6:1136082..1213994hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3877913
hg1977913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1161e214
Supporting Variantsessv12172254, essv12172253
SamplesHG03917, HG04033
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607882
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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