A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641107



Internal ID7027881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68070750..68082075hg38UCSC Ensembl
Innerchr17:68070778..68082048hg38UCSC Ensembl
Outerchr17:68070723..68082103hg38UCSC Ensembl
chr17:66066866..66078189hg19UCSC Ensembl
Innerchr17:66066894..66078162hg19UCSC Ensembl
Outerchr17:66066839..66078217hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3811326
hg1911324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15730481
SamplesHG00672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641107
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