A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585728



Internal ID6973249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36027592..36032854hg38UCSC Ensembl
Innerchr1:36027642..36032804hg38UCSC Ensembl
Outerchr1:36027542..36032904hg38UCSC Ensembl
chr1:36493193..36498455hg19UCSC Ensembl
Innerchr1:36493243..36498405hg19UCSC Ensembl
Outerchr1:36493143..36498505hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385263
hg195263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9902669
SamplesNA12872
Known GenesAGO3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585728
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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