A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6463521



Internal ID9722723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34460514..34466915hg38UCSC Ensembl
Outerchr1:34460477..34466965hg38UCSC Ensembl
Innerchr1:34926115..34932516hg19UCSC Ensembl
Outerchr1:34926078..34932566hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386489
hg196489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664160
Supporting Variants
SamplesNA19473
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6463521
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