A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625034



Internal ID18576629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39568834..39635710hg38UCSC Ensembl
Innerchr4:39570454..39637330hg19UCSC Ensembl
Innerchr4:39246849..39313725hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3866877
hg1966877
hg1866877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997937
Supporting Variants
Samples
Known GenesMIR1273H, SMIM14, UGDH-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625034
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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