A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6245982



Internal ID9223385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168693103..168693219hg38UCSC Ensembl
chr4:169614254..169614370hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666909
Supporting Variants
SamplesHG00319
Known GenesPALLD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6245982
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