A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021855



Internal ID19111073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144967865..145072757hg38UCSC Ensembl
Innerchr8:146193251..146298143hg19UCSC Ensembl
Innerchr8:146164055..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38104893
hg19104893
hg18104893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7339n100
Supporting Variantsnssv3690878, nssv3690876, nssv3690880, nssv3690879, nssv3690877
Samples
Known GenesC8orf33, TMED10P1, ZNF252P, ZNF252P-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021855
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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