A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598656



Internal ID16386065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:75052851..75053542hg38UCSC Ensembl
Innerchr5:74348676..74349367hg19UCSC Ensembl
Innerchr5:74384432..74385123hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38692
hg19692
hg18692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9880n54
Supporting Variantsnssv1035099, nssv1035102, nssv1035098, nssv1035101, nssv1035100
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598656
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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