A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611352



Internal ID6998261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155784367..155807154hg38UCSC Ensembl
Innerchr6:155784369..155807153hg38UCSC Ensembl
Outerchr6:155784366..155807156hg38UCSC Ensembl
chr6:156105501..156128288hg19UCSC Ensembl
Innerchr6:156105503..156128287hg19UCSC Ensembl
Outerchr6:156105500..156128290hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3822788
hg1922788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12599694, essv12599693
SamplesNA19908, HG02107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611352
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer