A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015471



Internal ID18758005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88521483..89003078hg38UCSC Ensembl
Innerchr7:88150798..88632392hg19UCSC Ensembl
Innerchr7:87988734..88470328hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38481596
hg19481595
hg18481595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655200
Samples
Known GenesC7orf62, ZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015471
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