A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611229



Internal ID6998140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150302060..150305393hg38UCSC Ensembl
Innerchr6:150302060..150305393hg38UCSC Ensembl
Outerchr6:150301868..150305500hg38UCSC Ensembl
chr6:150623196..150626529hg19UCSC Ensembl
Innerchr6:150623196..150626529hg19UCSC Ensembl
Outerchr6:150623004..150626636hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383334
hg193334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12581204, essv12581203, essv12581202
SamplesNA19792, HG02879, NA19913
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611229
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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