A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664919



Internal ID9931024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:164626912..164630009hg38UCSC Ensembl
Outerchr2:164626755..164630162hg38UCSC Ensembl
Innerchr2:165483422..165486519hg19UCSC Ensembl
Outerchr2:165483265..165486672hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg383408
hg193408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv744e199
Supporting Variantsessv6484504
SamplesHG00692
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664919
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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