A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001043



Internal ID19090260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94692486..94720350hg38UCSC Ensembl
Innerchr1:95158042..95185906hg19UCSC Ensembl
Innerchr1:94930630..94958494hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3827865
hg1927865
hg1827865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3466109
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)nsv1001043
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer