A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610064



Internal ID6996983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96037542..96044490hg38UCSC Ensembl
Innerchr6:96037582..96044450hg38UCSC Ensembl
Outerchr6:96037502..96044530hg38UCSC Ensembl
chr6:96485418..96492366hg19UCSC Ensembl
Innerchr6:96485458..96492326hg19UCSC Ensembl
Outerchr6:96485378..96492406hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386949
hg196949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12470595
SamplesHG01783
Known GenesFUT9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610064
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