A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011695



Internal ID18754229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15854885..15924038hg38UCSC Ensembl
Innerchr1:16181380..16250533hg19UCSC Ensembl
Innerchr1:16053967..16123120hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3869154
hg1969154
hg1869154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv38n100
Supporting Variantsnssv3471721
Samples
Known GenesSPEN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011695
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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