A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5540261



Internal ID8517664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12498463..12507882hg38UCSC Ensembl
Outerchr10:12498426..12507932hg38UCSC Ensembl
Innerchr10:12540462..12549881hg19UCSC Ensembl
Outerchr10:12540425..12549931hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg389507
hg199507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673513
Supporting Variants
SamplesNA18553
Known GenesCAMK1D
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5540261
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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