A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670087



Internal ID9589506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1653096..1715472hg38UCSC Ensembl
Outerchr1:1653096..1715507hg38UCSC Ensembl
Innerchr1:1583698..1646911hg19UCSC Ensembl
Outerchr1:1583664..1646946hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3862412
hg1963283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2e199
Supporting Variantsessv6457362
SamplesHG01354
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670087
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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