A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998181



Internal ID19157718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34434857..34511434hg38UCSC Ensembl
Innerchr2:34659924..34736501hg19UCSC Ensembl
Innerchr2:34513428..34590005hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3876578
hg1976578
hg1876578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3758n100
Supporting Variantsnssv3580955, nssv3728022, nssv3580953, nssv3728024, nssv3728025, nssv3580954, nssv3580956, nssv3728023, nssv3728021
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)nsv998181
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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