A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970368



Internal ID18605591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139582651..139590050hg38UCSC Ensembl
Innerchr6:139903788..139911187hg19UCSC Ensembl
Innerchr6:139945481..139952880hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg387400
hg197400
hg187400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762812
SamplesHGDP00778
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970368
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer