A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6033299



Internal ID9249143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7718983..7721203hg38UCSC Ensembl
Outerchr10:7718946..7721253hg38UCSC Ensembl
Innerchr10:7760946..7763166hg19UCSC Ensembl
Outerchr10:7760909..7763216hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382308
hg192308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670009
Supporting Variants
SamplesNA12045
Known GenesITIH2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6033299
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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