A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980090



Internal ID18615290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117051625..117073704hg38UCSC Ensembl
Innerchr3:116770472..116792551hg19UCSC Ensembl
Innerchr3:118253162..118275241hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3822080
hg1922080
hg1822080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759360
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980090
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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