A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060280



Internal ID18802811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43362671..43455533hg38UCSC Ensembl
Innerchr19:43866823..43959685hg19UCSC Ensembl
Innerchr19:48558663..48651525hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3892863
hg1992863
hg1892863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724884, nssv3724885
Samples
Known GenesCD177, TEX101
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060280
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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