A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001014



Internal ID18743545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15826990..15895558hg38UCSC Ensembl
Innerchr1:16153485..16222053hg19UCSC Ensembl
Innerchr1:16026072..16094640hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3868569
hg1968569
hg1868569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv37n100
Supporting Variantsnssv3464959
Samples
Known GenesFLJ37453, SPEN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001014
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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