A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005668



Internal ID19094885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48171930..48184712hg38UCSC Ensembl
Innerchr4:48173947..48186729hg19UCSC Ensembl
Innerchr4:47868704..47881486hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3812783
hg1912783
hg1812783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5203n100
Supporting Variantsnssv3625137
Samples
Known GenesTEC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005668
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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