A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972231



Internal ID18607447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66191957..66201779hg38UCSC Ensembl
Innerchr8:67104192..67114014hg19UCSC Ensembl
Innerchr8:67266746..67276568hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg389823
hg199823
hg189823
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759011
SamplesHGDP01284
Known GenesLINC00967
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972231
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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