A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8931176



Internal ID14997192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90367840..90367880hg38UCSC Ensembl
Innerchr6:90367841..90367877hg38UCSC Ensembl
Outerchr6:90367801..90367917hg38UCSC Ensembl
chr6:91077559..91077599hg19UCSC Ensembl
Innerchr6:91077560..91077596hg19UCSC Ensembl
Outerchr6:91077520..91077636hg19UCSC Ensembl
chr6:91134280..91134320hg18UCSC Ensembl
Innerchr6:91134317..91134281hg18UCSC Ensembl
Outerchr6:91134241..91134357hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38277
hg19277
hg18277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3373709
Supporting Variants
SamplesNA19225
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8931176
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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