A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249254



Internal ID21306159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78811345..78818857hg38UCSC Ensembl
Outerchr6:78810972..78821538hg38UCSC Ensembl
Innerchr6:79521062..79528574hg19UCSC Ensembl
Outerchr6:79520689..79531255hg19UCSC Ensembl
Innerchr6:79577781..79585293hg18UCSC Ensembl
Outerchr6:79577408..79587974hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810567
hg1910567
hg1810567
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169449
Supporting Variants
SamplesNGO_25
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249254
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