A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746664



Internal ID19044945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:165179528..165267492hg38UCSC Ensembl
Innerchr5:164606534..164694498hg19UCSC Ensembl
Innerchr5:164539112..164627076hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3887965
hg1987965
hg1887965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027103
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)nssv3746664
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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