A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581612



Internal ID18879893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45107394..45122212hg38UCSC Ensembl
Innerchr2:45334533..45349351hg19UCSC Ensembl
Innerchr2:45188037..45202855hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3814819
hg1914819
hg1814819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006369
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)nssv3581612
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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