A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014579



Internal ID18757114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16864355..16909763hg38UCSC Ensembl
Innerchr1:17190850..17236258hg19UCSC Ensembl
Innerchr1:17063437..17108845hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3845409
hg1945409
hg1845409
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109n100
Supporting Variantsnssv3700152, nssv3481718, nssv3471312, nssv3467321, nssv3471305, nssv3477275
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)nsv1014579
Frequency
Sample Size29084
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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