A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005371



Internal ID19094588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112140228..112163494hg38UCSC Ensembl
Innerchr1:112682850..112706116hg19UCSC Ensembl
Innerchr1:112484373..112507639hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3823267
hg1923267
hg1823267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv284n100
Supporting Variantsnssv3490584
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005371
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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