A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6396093



Internal ID8892378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7796730..7800299hg38UCSC Ensembl
Outerchr10:7796693..7800349hg38UCSC Ensembl
Innerchr10:7838693..7842262hg19UCSC Ensembl
Outerchr10:7838656..7842312hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383657
hg193657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671165
Supporting Variants
SamplesHG00342
Known GenesATP5C1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6396093
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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