A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972228



Internal ID18260758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8895187..8901517hg38UCSC Ensembl
Innerchr8:8752697..8759027hg19UCSC Ensembl
Innerchr8:8790107..8796437hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386331
hg196331
hg186331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763580
SamplesHGDP01307
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972228
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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