A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011191



Internal ID18753725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180163553..180222116hg38UCSC Ensembl
Innerchr1:180132688..180191251hg19UCSC Ensembl
Innerchr1:178399311..178457874hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3858564
hg1958564
hg1858564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv476n100
Supporting Variantsnssv3492816, nssv3497205, nssv3483193, nssv3499881, nssv3489900
Samples
Known GenesFLJ23867, QSOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011191
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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