A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585756



Internal ID6973277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37640549..37644665hg38UCSC Ensembl
Innerchr1:37640549..37644665hg38UCSC Ensembl
Outerchr1:37640474..37644748hg38UCSC Ensembl
chr1:38106221..38110337hg19UCSC Ensembl
Innerchr1:38106221..38110337hg19UCSC Ensembl
Outerchr1:38106146..38110420hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg384117
hg194117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9912679
SamplesHG03040
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585756
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