A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6420564



Internal ID9397967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163516033..163524586hg38UCSC Ensembl
Outerchr6:163515996..163524636hg38UCSC Ensembl
Innerchr6:163937065..163945618hg19UCSC Ensembl
Outerchr6:163937028..163945668hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg388641
hg198641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675455
Supporting Variants
SamplesHG00256
Known GenesQKI
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6420564
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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