A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016483



Internal ID19105702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8908421..8978418hg38UCSC Ensembl
Innerchr5:8908533..8978530hg19UCSC Ensembl
Innerchr5:8961533..9031530hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3869998
hg1969998
hg1869998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638104, nssv3638105
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016483
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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