A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013351



Internal ID18755882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66574047..66590254hg38UCSC Ensembl
Innerchr1:67039730..67055937hg19UCSC Ensembl
Innerchr1:66812318..66828525hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3816208
hg1916208
hg1816208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3474860
Samples
Known GenesSGIP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013351
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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