A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980493



Internal ID18615693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44015219..44024617hg38UCSC Ensembl
Innerchr4:44017236..44026634hg19UCSC Ensembl
Innerchr4:43711993..43721391hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg389399
hg199399
hg189399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759324
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980493
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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