A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6121590



Internal ID9098993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154592591..154596682hg38UCSC Ensembl
chr1:154565067..154569158hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg384092
hg194092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658585
Supporting Variants
SamplesHG01073
Known GenesADAR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6121590
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