A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5811543



Internal ID9711598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12151024..12151435hg38UCSC Ensembl
Outerchr10:12150848..12151588hg38UCSC Ensembl
Innerchr10:12193023..12193434hg19UCSC Ensembl
Outerchr10:12192847..12193587hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675175
Supporting Variants
SamplesNA19463
Known GenesSEC61A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5811543
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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