A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001152



Internal ID18743683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:239192375..239401382hg38UCSC Ensembl
Innerchr1:239355675..239564682hg19UCSC Ensembl
Innerchr1:237422298..237631305hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38209008
hg19209008
hg18209008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv594n100
Supporting Variantsnssv3705544, nssv3483999
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)nsv1001152
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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