A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012925



Internal ID19102142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94689978hg38UCSC Ensembl
Innerchr1:95130666..95155534hg19UCSC Ensembl
Innerchr1:94903254..94928122hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3824869
hg1924869
hg1824869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3468757, nssv3474438
Samples
Known GenesLINC01057
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012925
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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