A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002154



Internal ID19091371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:60243563..60282568hg38UCSC Ensembl
Innerchr1:60709235..60748240hg19UCSC Ensembl
Innerchr1:60481823..60520828hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3839006
hg1939006
hg1839006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3463461
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)nsv1002154
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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