A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169503



Internal ID21313986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41936745..41945921hg38UCSC Ensembl
Outerchr6:41934317..41947405hg38UCSC Ensembl
Innerchr6:41904483..41913659hg19UCSC Ensembl
Outerchr6:41902055..41915143hg19UCSC Ensembl
Innerchr6:42012461..42021637hg18UCSC Ensembl
Outerchr6:42010033..42023121hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3813089
hg1913089
hg1813089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245000
SamplesNGO_28
Known GenesCCND3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169503
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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