A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169400



Internal ID21313883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10068077..10069647hg38UCSC Ensembl
Outerchr6:10067770..10072210hg38UCSC Ensembl
Innerchr6:10068310..10069880hg19UCSC Ensembl
Outerchr6:10068003..10072443hg19UCSC Ensembl
Innerchr6:10176296..10177866hg18UCSC Ensembl
Outerchr6:10175989..10180429hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg384441
hg194441
hg184441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243965
SamplesMLY_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169400
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