A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579549



Internal ID18531144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:95660358..96019128hg38UCSC Ensembl
Innerchr2:96326106..96684876hg19UCSC Ensembl
Innerchr2:95689833..96048603hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38358771
hg19358771
hg18358771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003371
Supporting Variants
Samples
Known GenesFAHD2CP, LINC00342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579549
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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