A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001667



Internal ID18744198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61942114..62184166hg38UCSC Ensembl
Innerchr1:62407786..62649838hg19UCSC Ensembl
Innerchr1:62180374..62422426hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38242053
hg19242053
hg18242053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3468307, nssv3468068
Samples
Known GenesINADL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001667
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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