A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746648



Internal ID19044929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:145147630..145190494hg38UCSC Ensembl
Innerchr5:144527193..144570057hg19UCSC Ensembl
Innerchr5:144507386..144550250hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3842865
hg1942865
hg1842865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030271
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)nssv3746648
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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