A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981350



Internal ID18269862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:7277821..7548705hg38UCSC Ensembl
Innerchr6:7278054..7548938hg19UCSC Ensembl
Innerchr6:7223053..7493937hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38270885
hg19270885
hg18270885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764155
SamplesHGDP00542
Known GenesCAGE1, DSP, RIOK1, SSR1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981350
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