A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000636



Internal ID19089853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13984879..14044250hg38UCSC Ensembl
Innerchr1:14311374..14370745hg19UCSC Ensembl
Innerchr1:14183961..14243332hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3859372
hg1959372
hg1859372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n100
Supporting Variantsnssv3477868, nssv3472853, nssv3478768, nssv3472321
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)nsv1000636
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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