A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6277920



Internal ID9436297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:52650493..52651044hg38UCSC Ensembl
Outerchr1:52650456..52651094hg38UCSC Ensembl
Innerchr1:53116165..53116716hg19UCSC Ensembl
Outerchr1:53116128..53116766hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672204
Supporting Variants
SamplesNA18636
Known GenesFAM159A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6277920
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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