A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998659



Internal ID19158195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062181..13142703hg38UCSC Ensembl
Innerchr2:13202306..13282828hg19UCSC Ensembl
Innerchr2:13119757..13200279hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3880523
hg1980523
hg1880523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3718n100
Supporting Variantsnssv3577031, nssv3577033, nssv3577030, nssv3577032
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)nsv998659
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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