A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011325



Internal ID18753859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:161429698..161480024hg38UCSC Ensembl
Innerchr2:162286209..162336535hg19UCSC Ensembl
Innerchr2:161994455..162044781hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3850327
hg1950327
hg1850327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4097n100
Supporting Variantsnssv3582994
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)nsv1011325
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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