A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746161



Internal ID19044442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:4954453..4993470hg38UCSC Ensembl
Innerchr5:4954566..4993583hg19UCSC Ensembl
Innerchr5:5007566..5046583hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3839018
hg1939018
hg1839018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028717
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)nssv3746161
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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