A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063863



Internal ID19153082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46135838..46286792hg38UCSC Ensembl
Innerchr17:44213204..44364158hg19UCSC Ensembl
Innerchr17:41568981..41719935hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38150955
hg19150955
hg18150955
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3195n100
Supporting Variantsnssv3550096, nssv3550094, nssv3550100, nssv3550102, nssv3723866, nssv3550095, nssv3723865, nssv3550092, nssv3550103, nssv3550097, nssv3550101, nssv3550098, nssv3550099, nssv3723867, nssv3550093, nssv3550090, nssv3550091
Samples
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063863
Frequency
Sample Size11257
Observed Gain13
Observed Loss4
Observed Complex0
Frequencyn/a


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