A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018920



Internal ID18761453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88521483..90256991hg38UCSC Ensembl
Innerchr7:88150798..89886305hg19UCSC Ensembl
Innerchr7:87988734..89724241hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381735509
hg191735508
hg181735508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6525n100
Supporting Variantsnssv3655203, nssv3655202
Samples
Known GenesC7orf62, C7orf63, DPY19L2P4, STEAP1, STEAP2, ZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018920
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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