A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6549564



Internal ID9526967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91103277..91173399hg38UCSC Ensembl
chr8:92115505..92185627hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3870123
hg1970123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656822
Supporting Variants
SamplesHG00361
Known GenesLRRC69
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6549564
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