A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611256



Internal ID6651475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151192993..151197039hg38UCSC Ensembl
Innerchr6:151193002..151197030hg38UCSC Ensembl
Outerchr6:151192984..151197048hg38UCSC Ensembl
chr6:151514128..151518174hg19UCSC Ensembl
Innerchr6:151514137..151518165hg19UCSC Ensembl
Outerchr6:151514119..151518183hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384047
hg194047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12583976, essv12583972, essv12583973, essv12583975, essv12583978, essv12583974, essv12583977
SamplesNA20877, HG03968, NA20845, HG03697, NA18950, HG02681, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611256
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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