A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611441



Internal ID6998350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160590787..160595436hg38UCSC Ensembl
Innerchr6:160591287..160594936hg38UCSC Ensembl
Outerchr6:160589787..160596436hg38UCSC Ensembl
chr6:161011819..161016468hg19UCSC Ensembl
Innerchr6:161012319..161015968hg19UCSC Ensembl
Outerchr6:161010819..161017468hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg384650
hg194650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12612171, essv12612172
SamplesHG02562, NA20278
Known GenesLPA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611441
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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