A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603200



Internal ID6643456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:172661416..172662194hg38UCSC Ensembl
Innerchr4:172661419..172662191hg38UCSC Ensembl
Outerchr4:172661413..172662197hg38UCSC Ensembl
chr4:173582567..173583345hg19UCSC Ensembl
Innerchr4:173582570..173583342hg19UCSC Ensembl
Outerchr4:173582564..173583348hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11705023
SamplesHG02002
Known GenesGALNTL6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603200
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