A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023951



Internal ID18766484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17769986..17957752hg38UCSC Ensembl
Innerchr8:17627495..17815261hg19UCSC Ensembl
Innerchr8:17671775..17859541hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38187767
hg19187767
hg18187767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7121n100
Supporting Variantsnssv3684181
Samples
Known GenesFGL1, MTUS1, PCM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023951
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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