A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6309905



Internal ID9287308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35191377..35192722hg38UCSC Ensembl
Outerchr10:35191340..35192772hg38UCSC Ensembl
Innerchr10:35480305..35481650hg19UCSC Ensembl
Outerchr10:35480268..35481700hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381433
hg191433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668859
Supporting Variants
SamplesNA12003
Known GenesCREM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6309905
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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