A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005354



Internal ID18747885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58817900..59070140hg38UCSC Ensembl
Innerchr1:59283572..59535812hg19UCSC Ensembl
Innerchr1:59056160..59308400hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38252241
hg19252241
hg18252241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3473533
Samples
Known GenesLINC01135
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005354
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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