A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963557



Internal ID18598798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194838827..194849054hg38UCSC Ensembl
Innerchr3:194559556..194569783hg19UCSC Ensembl
Innerchr3:196040845..196051072hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3810228
hg1910228
hg1810228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2760149
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963557
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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