A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667617



Internal ID9587036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107658444..107659788hg38UCSC Ensembl
Outerchr1:107658407..107659838hg38UCSC Ensembl
Innerchr1:108201066..108202410hg19UCSC Ensembl
Outerchr1:108201029..108202460hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5636022
SamplesNA19703
Known GenesVAV3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667617
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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