A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014029



Internal ID19103249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14627792..14887321hg38UCSC Ensembl
Innerchr1:14954288..15213817hg19UCSC Ensembl
Innerchr1:14826875..15086404hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38259530
hg19259530
hg18259530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv35n100
Supporting Variantsnssv3477998
Samples
Known GenesKAZN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014029
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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