A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966222



Internal ID18601452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133252947..133271290hg38UCSC Ensembl
Innerchr4:134174102..134192445hg19UCSC Ensembl
Innerchr4:134393552..134411895hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3818344
hg1918344
hg1818344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763373
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966222
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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