A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2759360



Internal ID17858665
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv980090
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2759360
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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