A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153945



Internal ID15531332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81735922..82195268hg38UCSC Ensembl
Innerchr5:81031741..81491087hg19UCSC Ensembl
Innerchr5:81067497..81526843hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38459347
hg19459347
hg18459347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598753
Supporting Variants
SamplesHGDP01084
Known GenesATG10, SSBP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153945
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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