A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006061



Internal ID22067692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:85578668..85594141hg38UCSC Ensembl
Outerchr10:85575450..85599298hg38UCSC Ensembl
Innerchr10:87338425..87353898hg19UCSC Ensembl
Outerchr10:87335207..87359055hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3823849
hg1923849
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154638
Supporting Variants
Samples
Known GenesGRID1-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006061
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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