A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153537



Internal ID15855194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45364773..45456975hg38UCSC Ensembl
Innerchr5:45364875..45457077hg19UCSC Ensembl
Innerchr5:45400632..45492834hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3892203
hg1992203
hg1892203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597981
Supporting Variants
Samples1780862470_A
Known GenesHCN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153537
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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