A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585754



Internal ID6973275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37590655..37591681hg38UCSC Ensembl
Innerchr1:37590688..37591649hg38UCSC Ensembl
Outerchr1:37590623..37591714hg38UCSC Ensembl
chr1:38056256..38057282hg19UCSC Ensembl
Innerchr1:38056289..38057250hg19UCSC Ensembl
Outerchr1:38056224..38057315hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9910307
SamplesHG03159
Known GenesGNL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585754
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