A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608791



Internal ID6649024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41595290..41596678hg38UCSC Ensembl
Innerchr6:41595290..41596678hg38UCSC Ensembl
Outerchr6:41595168..41596852hg38UCSC Ensembl
chr6:41563028..41564416hg19UCSC Ensembl
Innerchr6:41563028..41564416hg19UCSC Ensembl
Outerchr6:41562906..41564590hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12327728, essv12327730, essv12327731, essv12327726, essv12327729, essv12327727, essv12327732
SamplesHG02450, HG03301, NA20321, NA20320, HG03118, NA19138, NA19025
Known GenesFOXP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608791
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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