A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015241



Internal ID22076872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:50063167..50073927hg38UCSC Ensembl
Outerchr1:50062919..50077250hg38UCSC Ensembl
Innerchr1:50528839..50539599hg19UCSC Ensembl
Outerchr1:50528591..50542922hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3814332
hg1914332
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155825
Supporting Variants
Samples
Known GenesELAVL4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015241
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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