A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011358



Internal ID22072989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82850073..82963919hg38UCSC Ensembl
Outerchr2:82847483..82966495hg38UCSC Ensembl
Innerchr2:83077197..83191043hg19UCSC Ensembl
Outerchr2:83074607..83193619hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38119013
hg19119013
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155751
Supporting Variants
Samples
Known GenesLOC1720
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011358
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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