A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6159332



Internal ID9456994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41606044..41606932hg38UCSC Ensembl
chr1:42071715..42072603hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657722
Supporting Variants
SamplesNA18908
Known GenesHIVEP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6159332
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