A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008828



Internal ID18751359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15826990..15917908hg38UCSC Ensembl
Innerchr1:16153485..16244403hg19UCSC Ensembl
Innerchr1:16026072..16116990hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3890919
hg1990919
hg1890919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv37n100
Supporting Variantsnssv3482289
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)nsv1008828
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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