A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014015



Internal ID18756547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:175461063..175783051hg38UCSC Ensembl
Innerchr1:175430199..175752187hg19UCSC Ensembl
Innerchr1:173696822..174018810hg18UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38321989
hg19321989
hg18321989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv466n100
Supporting Variantsnssv3496225
Samples
Known GenesTNR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014015
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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