A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608052



Internal ID6994982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9589417..9595777hg38UCSC Ensembl
Innerchr6:9589417..9595777hg38UCSC Ensembl
Outerchr6:9588917..9596277hg38UCSC Ensembl
chr6:9589650..9596010hg19UCSC Ensembl
Innerchr6:9589650..9596010hg19UCSC Ensembl
Outerchr6:9589150..9596510hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg386361
hg196361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12185802
SamplesHG02471
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608052
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer