A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006601



Internal ID19095818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:164104484..164162308hg38UCSC Ensembl
Innerchr1:164073721..164131545hg19UCSC Ensembl
Innerchr1:162340345..162398169hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3857825
hg1957825
hg1857825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704811
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)nsv1006601
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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