A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6429796



Internal ID9407199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12078136..12081575hg38UCSC Ensembl
Outerchr10:12077979..12081728hg38UCSC Ensembl
Innerchr10:12120135..12123574hg19UCSC Ensembl
Outerchr10:12119978..12123727hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383750
hg193750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658955
Supporting Variants
SamplesHG00285
Known GenesDHTKD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6429796
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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