A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587985



Internal ID6975409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175267734..175270164hg38UCSC Ensembl
Innerchr1:175267734..175270164hg38UCSC Ensembl
Outerchr1:175267641..175270266hg38UCSC Ensembl
chr1:175236870..175239300hg19UCSC Ensembl
Innerchr1:175236870..175239300hg19UCSC Ensembl
Outerchr1:175236777..175239402hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10190896
SamplesNA11932
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587985
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