A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965590



Internal ID18600820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:76765258..76785591hg38UCSC Ensembl
Innerchr5:76061083..76081416hg19UCSC Ensembl
Innerchr5:76096839..76117172hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3820334
hg1920334
hg1820334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763365
SamplesHGDP01284
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965590
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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