A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060887



Internal ID18803418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7089546..7861087hg38UCSC Ensembl
Innerchr19:7089557..7925973hg19UCSC Ensembl
Innerchr19:7040557..7831973hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38771542
hg19836417
hg18791417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723279
Samples
Known GenesARHGEF18, C19orf45, C19orf59, CAMSAP3, CD209, CLEC4G, CLEC4GP1, CLEC4M, EVI5L, FCER2, INSR, LOC100128573, MCOLN1, MIR6792, PCP2, PET100, PEX11G, PNPLA6, RETN, STXBP2, TRAPPC5, XAB2, ZNF358
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060887
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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