A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765082



Internal ID17488654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8015970..8025658hg38UCSC Ensembl
Innerchr10:8057933..8067621hg19UCSC Ensembl
Innerchr10:8097939..8107627hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389689
hg199689
hg189689
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975059
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765082
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