A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624302



Internal ID6664469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96657845..96660953hg38UCSC Ensembl
Innerchr10:96657845..96660953hg38UCSC Ensembl
Outerchr10:96657722..96661079hg38UCSC Ensembl
chr10:98417602..98420710hg19UCSC Ensembl
Innerchr10:98417602..98420710hg19UCSC Ensembl
Outerchr10:98417479..98420836hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg383109
hg193109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13905578, essv13905579
SamplesNA19401, HG02318
Known GenesPIK3AP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624302
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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