A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664104



Internal ID9930209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:39819603..39821116hg38UCSC Ensembl
Outerchr1:39819446..39821269hg38UCSC Ensembl
Innerchr1:40285275..40286788hg19UCSC Ensembl
Outerchr1:40285118..40286941hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381824
hg191824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39e199
Supporting Variantsessv6326102
SamplesNA18988
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664104
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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