A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970366



Internal ID18605589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73996489..74013903hg38UCSC Ensembl
Innerchr6:74706205..74723619hg19UCSC Ensembl
Innerchr6:74762925..74780339hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3817415
hg1917415
hg1817415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762981
SamplesHGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970366
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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