A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018078



Internal ID19107295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113279523..113321707hg38UCSC Ensembl
Innerchr5:112615220..112657404hg19UCSC Ensembl
Innerchr5:112643119..112685303hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3842185
hg1942185
hg1842185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647061
Samples
Known GenesMCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018078
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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