A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155837



Internal ID22086342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:95065229..95069721hg38UCSC Ensembl
Outerchr2:95050220..95071934hg38UCSC Ensembl
Innerchr2:95730974..95735466hg19UCSC Ensembl
Outerchr2:95715965..95737679hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3821715
hg1921715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013123, nssv4013127, nssv4013126, nssv4013122, nssv4013125, nssv4013124
Samples
Known GenesMAL
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155837
Frequency
Sample Size131
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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