A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639855



Internal ID6679945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6987653..6989956hg38UCSC Ensembl
Innerchr17:6987665..6989945hg38UCSC Ensembl
Outerchr17:6987642..6989968hg38UCSC Ensembl
chr17:6890972..6893275hg19UCSC Ensembl
Innerchr17:6890984..6893264hg19UCSC Ensembl
Outerchr17:6890961..6893287hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382304
hg192304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15602866
SamplesHG03718
Known GenesLOC100506713
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639855
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