A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744521



Internal ID19042802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:175077424..175318559hg38UCSC Ensembl
Innerchr4:175998575..176239710hg19UCSC Ensembl
Innerchr4:176235150..176476705hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38241136
hg19241136
hg18241556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016576
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)nssv3744521
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer