A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635951



Internal ID18934232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24778255..24789210hg38UCSC Ensembl
Innerchr5:24778364..24789319hg19UCSC Ensembl
Innerchr5:24814121..24825076hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3810956
hg1910956
hg1810956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016850
Supporting Variants
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)nssv3635951
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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