A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016187



Internal ID22077818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226478072..226481352hg38UCSC Ensembl
Outerchr2:226477322..226483083hg38UCSC Ensembl
Innerchr2:227342788..227346068hg19UCSC Ensembl
Outerchr2:227342038..227347799hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg385762
hg195762
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155921
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016187
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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